Method for identification and detection of microorganisms using gyrase gene as an indicator

ABSTRACT

With the nucleotide sequence of gyr B, it is possible to classify or identify an unidentified microorganism strain quickly and accurately. Furthermore, PCR primers for monitoring a specific microorganism, which are needed in risk assessment in various bioprocesses, can be designed easily. Also, changes in mycelial tufts can be accurately monitored.

BACKGROUND OF THE INVENTION

[0001] 1. Field of the Invention

[0002] The present invention is involved in a method for the identification and detection of organisms using the sequences of their genes encoding the B subunit of the DNA gyrase.

[0003] This invention is useful in medical fields as well as various industrial fields where the identification/classification or detection/monitoring of specific microorganisms (bacteria, yeasts, fungi, archaea and bacteria), especially bacteria, is necessary.

[0004] 2. Prior Art

[0005] Conventionally, the identification/classification of living organisms has been carried out using the combination of biochemical and morphological tests. However, these tests often did not provide unequivocal answers to the taxonomic positions of tested organisms.

[0006] Recently, the taxonomy of organisms, in particular of bacteria, using rRNA sequences became fashionable. There are many reasons why rRNA molecules have been selected as standard molecules for the molecular taxonomy. They are constituents of all organisms. They exist in abundance, and therefore, can readily be isolated and characterized. For sequence comparison, many conserved regions of rRNA molecules allowed the alignment between distantly related organisms, while variable regions are useful for the distinction of closely related organisms (van de Peer, Y., S. Chapelles, and R. de Wacher. 1996. A quantitative map of nucleotide substitution rates in bacterial rRNA. Nucleic Acids Res. 24: 3381-3391; and Gutell, R. R., N. Larsen, and C. R. Woese. 1994. Lessons from an evolving rRNA: 16S and 23S rRNA structures from a comparative perspective. Microbiol. Rev. 58: 10-26). Furthermore, there is a few evidence for the horizontal transfer of rRNA genes although many other genes are expected to have frequently been transferred from one species to other distantly related species. At present, rRNA sequences are accumulating rapidly and they are accessible via an international database (Ribosomal Database project, http://rdp.life.uiuc.edu/).

[0007] However, as is clear from the fact that the evolution speed of rRNA genes is extremely slow, there is little difference in the rRNA sequences between closely related organisms. Therefore, in many times, species belonging to the same genus could not be discriminated by the analysis using rRNA sequences. For example, it is said that bacteria sharing more than 97% of identity in their 16S rRNA sequences (bacterial small subunit rRNA) might belong to the same species. However, there are cases of bacteria exhibiting more than 99% identity in their 16S rRNA sequences, and yet belonging to two distinct species as revealed from DNA hybridization analysis. Evidently, due to the slow speed of divergent evolution of the 16S rRNA gene, the resolution of 16S rRNA-based analysis between closely related organisms is lower than that of DNA hybridization analysis (Stackebrandt, E. and Goebel, B. M. 1994. Taxonomic note: a place far DNA-DNA reassociation and 16S rRNA sequence analysis in the present species difinition in bacteriology. Int. J. Syst. Bacteriol. 37: 463-464).

[0008] Other problems exist in the rRNA-based phylogenetic analysis. To establish a phylogenetic relationship based on rRNA sequences, these sequences should be aligned. The alignment of rRNA sequences composed from four different constituents (AUCG), however, is not easy, and requires some expertise. The correct sequencing of rRNA genes is also difficult largely due to their highly ordered structure. Furthermore, polymorphism of rRNA was found in some organisms.

[0009] In contrast, protein-encoding genes have evolved more rapidly than rRNA-encoding genes, since they allow the so-called neutral mutations that do not cause any amino acid substitutions in their gene products. It is then expected that, by using such protein-encoding genes, more precise phylogenetic analysis can be performed than by using rRNA sequences. Thus, the present inventors have developed and applied a method for the identification/classification or detection/monitoring of organisms using the sequences of gyr B genes encoding the B subunit of DNA gyrases (Yamamoto, S. and Harayama, S. 1995. PCR Amplification and Direct Sequencing of gyr B Genes with Universal Primers and Their Application to the Detection and Taxonomic Analysis of Pseudomonas putida Strains. Appl. Environ. Microbiol. 61: 1104-1109; Yamamoto, S. and Harayama, S. 1996. Phylogenetic Analysis of Acinetobacter Strains Based on the Nucleotide Sequences of gyr B Genes and on the Amino acid Sequences of Their Products. Int. J. Syst Bacteriol. 46: 506-511; Yamamoto, S. and Harayama S. 1998. Phylogenetic relationships of Pseudomonas putida strains deduced from the nucleotide sequences of gyr B, rpoD and 16S rRNA genes. Int. J. Syst Bacteriol. 48: 813-819; Yamamoto S., Bouvet P. J. M. & Harayama, S. 1998. Phylogenetic structures of the genus Acinetobacter based on the gyr B sequences: Comparison with the grouping by DNA-DNA hybridization. Int. J. Syst. Bacteriol. (in press); Harayama, S. and Yamamoto, S. 1996. P hylogenetic Identification of Pseudomonas Strains Based on a Comparison of gyr B and rpoD Sequences. p. 250-258 in Molecular Biology of Pseudomonads, edited by T, Nakazawa, K. Furukawa, D Haas, S. Silver. ASM Press, Washington, D.C.: and Watanabe, K., Yamamoto, S., Hino, S. and Harayama, S. 1998. Population dynamics of phenol-degrading bacteria in activated sludge determined by gyr B-targeted quantitative PCR. Appl. Environ. Microbiol. 64: 1203-1209).

[0010] DNA topoisomerases are essential for the replication, transcription, recombination and repair of DNA and control the level of supercoiling of DNA molecules by cleaving and resealing the phosphodiester bond of DNA. They are classified into type I (EC 5.99. 1.2) and type II (EC 5.99.1.3) according to their enzymatic properties. The DNA gyrase is a type II topoisomerase that is capable of introducing negative supercoiling into a relaxed closed circular DNA molecule. This reaction is coupled with ATP hydrolysis. DNA gyrase can also relax supercoiled DNA without ATP hydrolysis. DNA gyrase consists of two subunit proteins in the quaternary structure of A2B2. The A subunit (GyrA) has a molecular weight of approximately 100 kDa while the B subunit (GyrB) has a molecular weight of either 90 kDa or 70 kDa (Wigley, D. B. 1995. Structure and mechanism of DNA topoisomerases. Ann. Rev. Biomol. Struct. 24: 185-208). The genes for DNA gyrase or its isofunctional enzymes should exist in all organisms as they are indispensable for the cell proliferation.

[0011] As described above, the present Inventors have already developed and applied successfully the method for the identification/classification or detection/monitoring of organisms using gyr B sequences. In this method, a gyr B gene fragment of an organism of interest is amplified by PCR using primers designed from the two amino acid sequences, His-Ala-Gly-Gly-Lys-Phe-Asp and Met-Thr-Asp-Ala-Asp-Val-Asp-Gly, which are highly conserved among the GyrB sequences of many organisms. Subsequently, the amplified fragments are subjected to direct sequencing. Since the gyr B genes code for proteins, they have frequently undergone neutral mutations. Thus, the nucleotide sequence of the gyr B genes vary considerable even among related organisms. For this reason, the above method has been shown to be effective for discriminating organisms at a level of species of subspecies.

[0012] The above-mentioned PCR primers designed from the highly conserved amino acid sequences of GyrB were effective in many but not all bacterial species for the PCR amplification of gyr B. From DNA of some bacterial species, no PCR amplification was observed using these primers.

[0013] Besides, there was another problem associated with these primers. The genes for type IV topoisomerese (ParE) were also amplified from DNA of some bacterial species by using these primers. Topoisomerase IV (ParE) is a bacterial enzyme that appears to be closely related to DNA gyrase. This enzyme involves in the partition of chromosomes into daughter cells. If a ParE gene but not gyr B gene is amplified from a DNA, and if a phylogenetic analysis is carried out without recognizing that the amplified sequence is parE but not gyr B, it will bring some confusion to the phylogenetic analysis. To avoid such problem associated with the amplification of paralogous genes, primers which do not amplify ParE should be developed.

OBJECTIVE AND SUMMARY OF THE INVENTION

[0014] It is an object of the present invention to solve the above-described problems of the primers and to provide a means which enables the identification/classification and detection/monitoring of a wide range of organisms using gyr B sequences.

[0015] Comparing the amino acid sequence data of GyrB collected by the inventors with those of ParE, the inventors have found that a gyrB gene DNA fragment only can be isolated from a wide range of microorganisms by performing PCR using two specific primers (forward and reverse primers), thereby completing the present invention.

[0016] First, the present invention relates to a method for the indentification and detection of a microorganism, comprising the following steps (1) to (5):

[0017] (1) synthesizing two specific primers,

[0018] (2) amplifying gyrB gene DNA from the microorganism using the above two primers to produce a gyrB gene DNA fragment,

[0019] (3) isolating the above DNA fragment,

[0020] (4) determining the nucleotide sequence of the above DNA fragment, and

[0021] (5) identifying and detecting the microorganism by comparing the nucleotide sequence of the amplified gyrB gene DNA fragment to known gyrB gene DNA fragment sequences.

[0022] Second, the present invention relates to a method for the identification and detection of a microorganism, comprising the following steps (1) to (7):

[0023] (1) synthesizing two specific primers,

[0024] (2) amplifying gyrB gene DNA from the microorganism using the above two primers to produce a gyrB gene DNA fragment,

[0025] (3) synthesizing two pairs of specific primers,

[0026] (4) amplifying the gyrB gene DNA fragment produced in step (2) using the above two pairs of primers to produce two gyrB gene DNA fragments,

[0027] (5) isolating the above two DNA fragments,

[0028] (6) determining the nucleotide sequences of the above two DNA fragments, and

[0029] (7) identifying and detecting the microorganism by comparing the nucleotide sequences of the above two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.

[0030] Third, the present invention relates to a method for the indentification and detection of a microorganism, comprising the following steps (1) to (5):

[0031] (1) synthesizing two pairs of specific primers,

[0032] (2) amplifying gyrB gene DNA from the microorganism using the above two pairs of primers to produce gyrB gene DNA fragments,

[0033] (3) isolating the above two DNA fragments,

[0034] (4) determining the nucleotide sequences of the above two DNA fragments, and

[0035] (5) identifying the microorganism by comparing the nucleotide sequences of the above two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.

BRIEF DESCRIPTION OF THE DRAWINGS

[0036]FIG. 1 shows the locational relationship between the amino acid sequence (a) through (l) and the amino acid sequences of GyrB of several organisms.

DETAILED DESCRIPTION OF THE INVENTION

[0037] Hereinbelow, the present invention will be described in detail.

[0038] The method for identification and detection of a microorganism of the present invention is a method for identifying and detecting of a microorganism based on the nucleotide sequence of a gyrB gene. The nucleotide sequence data of a gyrB gene may be obtained from a DNA fragment amplified by PCR (one fragment method), or may be obtained from two fragments having a mutually overlapping portion (two fragments method).

[0039] In order to identify and detect a microorganism with high accuracy, a nucleotide sequence of approx. 1 kb DNA fragment is required. In 1994, Yamamoto and Harayama filed a patent application for an invention relating to primers to amplify a gyrB fragment, which is a gene encoding the B subunit of DNA gyrases (Japanese Patent Application Laid-Open (Kokai) No. 1995-213299). However, the subsequent study has clarified that, according to the disclosure of the above application alone, the identification and detection of a microorganism may be difficult for the following reasons:

[0040] (1) It is difficult to determine a nucleotide sequence by a one-time sequencing reaction.

[0041] (2) Some strains are inefficiently amplified with only the known primer sequences.

[0042] (3) In some cases, it is difficult to determine a nucleotide sequence, since parE, being a homologous gene of gyrB, is amplified together with gyrB. In other cases, an incorrect identification of a microorganism is performed, since parE is selectively amplified.

[0043] To overcome the above-stated problems, in addition to the primer sequences disclosed by Yamamoto and Harayama in 1995, the present invention provides: primer sequences conserved among gyrB genes of a large number of bacteria; primer sequences specific for gyrB genes, not appearing in parE genes, or primer sequences appearing in both gyrB and parE genes, which allow easy distinction of an amplified parE fragment from an amplified gyrB fragment; and a method for specific amplification of a gyrB gene by the combined use of the above primer sequences.

[0044] To overcome the above-stated problems, sometimes it may be more preferable to amplify separately two DNA fragments having a mutually overlapping portion, and to determine the nucleotide sequence of each fragment, followed by connecting the obtained two sequences before using the data.

[0045] In order to amplify the two fragments, DNA obtained from the microorganism (which also contains various DNAs as well as gyrB gene DNA) may be used as is, as a template (“one step—two fragments method”), but as another option, after performing PCR using primers capable of specifically amplifying a gyrB gene DNA, the obtained amplified products may be used as a template (“two steps—two fragments method”).

[0046] Primers used for the above three types of DNA amplification methods (“one fragment method”, “one step—two fragments method” and “two steps—two fragments method”) are shown in FIG. 1. The FIGURE shows the amino acid sequence of each GyrB of 3 kinds of strains, Bacillus subtilis 168, Escherichia coli K-12 and Pseudomonas putida PRS2000, and (a)-(l) in the FIGURE respectively correspond to amino acid sequences (a)-(l) shown as follows:

[0047] (a) (Pro or Ser)-(Ala or Thr)-(Ala, Val or Leu)-Glu or Asp)-(Val or Thr)-(Ile or Val)-(Met, Leu or Phe)-Thr-(Val, Gln or Ile)-Leu-His-Ala-Gly-Gly-Lys-Phe-(Asp or Gly)-(Asp, Gly, Asn or Ser)-(Ser, Lys, Gly, Asp or Asn) [SEQ ID NO.69]

[0048] (b) Gly-Gly-Thr-His [SEQ ID NO.70]

[0049] (c) (Ile or Leu)-Met-Thr-Asp-Ala-Asp-Val-Asp-Gly-(Ala or Ser)-His-Ile-Arg-Thr-Leu [SEQ ID NO.71]

[0050] (d) Arg-Lys-Arg-Pro-(Gly or Ala)-Met-Tyr-Ile-Gly-(Ser or Asp)-Thr [SEQ ID NO.72]

[0051] (e) Gln-(Thr or Pro)-(Lys or Asn)-(Thr, Asp, Gly, Lys, Ser, Phe or Tyr)-Lys-Leu [SEQ ID NO.73]

[0052] (f) (Tyr or Phe)-Lys-Gly-Leu-Gly-Glu-Met-Asn-(Ala or Pro) [SEQ ID NO.74]

[0053] (g) Val-Glu-Gly-Asp-Ser-Ala-Gly-Gly-Ser [SEQ ID NO.75]

[0054] (h) Lys-(His or Val)-Pro-Asp-Pro-(Gln or Lys)-Phe [SEQ ID NO.76]

[0055] (i) Leu-Pro-Gly-Lys-Leu-Ala-Asp-Cys-(Ser or Gln)-(Ser or Glu)-(Lys or Arg)-Asp-Pro-(Ala or Ser) [SEQ ID NO.77]

[0056] (j) Gln-Leu-(Trp or Arg)-(Glu or Asp)-Thr-Thr-(Met or Leu)-(Asp or Asn)-Pro [SEQ ID NO.78]

[0057] (k) Ala-(Lys or Arg)-(Lys or Arg)-Ala-Arg-Glu [SEQ ID NO.79]

[0058] (l) Phe-Thr-Asn-Asn-Ile-(Pro or Asn)-(Thr or Gln) [SEQ ID NO.80].

[0059] Two primers used for the “one fragment method” include the ones which are synthesized based on a single pair of amino acid sequences selected from the group consisting of sequence pairs (a) and (f), (a) and (j), (d) and (c), (d) and (f), and (d) and (j). The gyrB gene of members of proteobacteria has an approx. 500 bp insertion sequence located between a sequence pair (c) and (f), and another sequence pair (c) and (j), on the other hand, parE which is a homologous gene thereof does not have such sequence (Kato, J.-i., Nishimura, Y., Imamura, R., Niki, H., Hiraga, S., and Suzuki, H. New topoisomerase essential for chromosome segregation in E. coli Cell 63, 393-404 (1990)). Accordingly, in a case where two primers synthesized based on amino acid sequence pairs (a) and (f), (a) and (j), (d) and (f), or (d) and (j) are used for identification and detection of a microorganism belonging to proteobacteria, DNA fragments of gyrB genes can easily be separated from those of parE genes by electrophoresis and so on, since the length of the amplified DNA fragments of the two types of genes is different.

[0060] Two primers used for the “one step—two fragments method” include the following amino acid sequence combinations: Amplified fragment 1 Amplified fragment 2 Combination 1 sequences (d) and (e) sequences (h) and (c), sequences (h) and (f), or sequences (h) and (g) Combination 2 sequences (a) and (i) sequences (k) and (c), sequences (k) and (f), or sequences (k) and (g) Combination 3 sequences (a) and (i) sequences (l) and (c), sequences (l) and (f), or sequences (l)and (g)

[0061] Among amino acid sequences in the above table, sequences (i), (e), (h), (k) and (l) do not exist in ParE, and in many cases, are specific for GyrB. For example, these sequences are determined to be specific for GyrB in the strains shown in the following table. Sequence Strain (i) Leclercia adecarboxylata GTC 1267 Pseudoalteromonas sp. A316 Gordonia amarae DSM 46078 Rhodococcus koreensis JCM 10743 Shigella dysenteriae GTC 786 Salmonella typhi P1 Sphingomonas sp. MBIC 5538 Serratia ficaria GTC 343 Alteromonas macleodii MBIC 1375 Vibrio fluvialis GTC 315 (e) Mycobacterium tuberculosis KPM T21 Bacteroides fragilis Acholeplasma laidlawii PG-8B Bacillus cereus JCM 2152 Treponema denticola ATCC 35405 Streptococcus pneumoniae 7785 Arthrobacter oxidans IFO 12138 Porphyromonas asaccharolytica JCM 6326 Myxococcus xanthus ER-15 Streptomyces coelicolor A3 (2) (h) Pseudomonas putida MBIC 5295 Pseudoalteromonas sp. MBIC 3307 Vibrio hollisae 89A 1962 Aeromonas hydrophila P3 Photobacterium histaminum JCM 8968 Escherichia coli W3110 Bacillus anthracis Pasteur #2 Streptococcus pneumoniae 7785 Acinetobacter calcoacelicus ATCC 23055 Acholeplasma laidlawii PG-8B (k) Pseudomonas putida MBIC 5295 Pseudoalteromonas sp. MBIC 3307 Vibrio hollisae 89A 1962 Citrobacter sp. MAM-1 Comamonas terrigena IAM 12052 Salmonella typhimurium Acinetobacter junii SEIP 14. 81 Legionella pneumophila ATCC 33152 Escherichia coli W3110 Photobacterium histaminum JCM 8968 (l) Leclercia adecarboxylata GTC 1267 Pseudoalteromonas sp. A316 Pseudomonas sp. MBIC 5390 Marinobacter sp. MBIC 4911 Shigella dysenteriae GTC 786 Salmonella typhi P1 Sphingomonas sp. MBIC 5538 Caulobacter sp. GTC 1043 Sinorhizobium fredi ATCC 35423 Comamonas sp. GTC 866

[0062] Accordingly, by performing PCR with the combined use of the above primers, the gyrB gene DNA only can be specifically amplified.

[0063] Two primers used for the “two steps—two fragments method” include the following amino acid sequence combinations: 2^(nd) amplification step 1^(st) amplification step fragment 1 fragment 2 Combination 1 sequences (a) and (c) sequences (a) and (e) sequences (b) and (c) Combination 2 sequences (a) and (f) sequences (a) and (e) sequences (b) and (f) Combination 3 sequences (d) and (t) sequences (d) and (e) sequences (b) and (f)

[0064] Among amino acid sequences in the above table, sequence (b) exists in GyrB of all known bacteria, and so primers synthesized based on this sequence can be applied for a wide range of microorganisms. Since sequence (b) consists of 4 amino acid residues, when PCR is performed using, as a template, DNA obtained from the microorganism with primers synthesized based on the sequence, there is a possibility to amplify DNA fragments totally irrelevant to gyrB genes. However, for the “two steps—two fragments method”, amplified gyrB gene DNA fragments are used as a template, and so the above non-specific amplification can be avoided.

[0065] Since sequence (f) is conserved in GyrB genes of many bacteria, primers synthesized based on this sequence can be applied for a wide range of microorganisms. Since sequence (f) exists also in ParE, when PCR is performed using this sequence, not only gyrB gene DNA fragments, but also parE gene DNA fragments are amplified. However, the amplification of parE gene DNA fragments can be prevented by performing PCR using primers synthesized based on sequence (e) specific for GyrB.

[0066] “Primers synthesized based on sequences (a)-(l)” mean primers encoding all or a part of amino acid sequences (a)-(l), and having a length sufficient to specifically hybridize to a specific site of a template DNA.

[0067] The nucleotide sequences of primers synthesized based on sequences (a)-(l) and amino acid sequences encoded by these nucleotide sequences are shown in the following table: Sequence Amino acid sequence Nucleotide sequence (a) SEQ ID NO: 26 SEQ ID NO: 25 SEQ ID NO: 30 SEQ ID NO: 29 SEQ ID NO: 54, 55, 56, 57 SEQ ID NO: 53 (b) SEQ ID NO: 34 SEQ ID NO: 33 SEQ ID NO: 36, 37 SEQ ID NO: 35 (c) SEQ ID NO: 28 SEQ ID NO: 27 SEQ ID NO: 32 SEQ ID NO: 31 SEQ ID NO: 42 SEQ ID NO: 41 (d) SEQ ID NO: 46, 47 SEQ ID NO: 45 (e) SEQ ID NO: 39, 40 SEQ ID NO: 38 (f) SEQ ID NO: 44 SEQ ID NO: 43 (g) SEQ ID NO: 49 SEQ ID NO: 48 (h) SEQ ID NO: 63, 64 SEQ ID NO: 62 (i) SEQ ID NO: 59 SEQ ID NO: 58 (j) SEQ ID NO: 66, 67, 68 SEQ ID NO: 65 (k) SEQ ID NO: 51, 52 SEQ ID NO: 50 (l) SEQ ID NO: 61 SEQ ID NO: 60

[0068] Microorganisms applicable to the identification and detection method of the present invention include bacteria, yeast, Fungus, archaebacteria and the like.

PREFERRED EMBODIMENTS OF THE INVENTION EXAMPLE 1

[0069] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 25 and 27 (corresponding to the amino acid sequences of SEQ ID NOS: 26 and 28, respectively) as primers and DNA from Bacteroides vulgatus IFO 14291 strain as a template. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 1 and 2, respectively. The PCR amplification conditions were as described below. PCR amplification conditions: 96° C. 1 min; 48° C. 1 min; 72° C. 2 min: 3 cycles 96° C. 1 min; 48° C. 1 min; 72° C. 2 min: 3 cycles 96° C. 1 min; 48° C. 1 min; 72° C. 2 min: 30 cycles Total: 36 cycles Primer concentration 1 μM each dATP 200 μM each Template DNA <1 μg/100 μl

EXAMPLE 2

[0070] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 29 and 31 (corresponding to the amino acid sequences of SEQ ID NOS: 30 and 32, respectively) as primers and DNA from Mycobacterium simiae KPM 1403 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 3 and 4, respectively.

EXAMPLE 3

[0071] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 33 and 27 (corresponding to the amino acid sequences of SEQ ID NOS: 34 and 28, respectively) as primers and DNA from Chitinophaga pinensis DSM 2588 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 5 and 6, respectively.

EXAMPLE 4

[0072] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 25 and 35 (corresponding to the amino acid sequences of SEQ ID NO: 26 and SEQ ID NO: 36 or 37, respectively) as primers and DNA from Flavobacterium aquatile IAM 12316 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 7 and 8, respectively.

EXAMPLE 5

[0073] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 29 and 38 (corresponding to the amino acid sequences of SEQ ID NO: 30 and SEQ ID NO: 39 or 40, respectively) as primers and DNA from Mycobacterium asiaticum ATCC 25274 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 9 and 10, respectively.

EXAMPLE 6

[0074] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 41 and 43 (corresponding to the amino acid sequences of SEQ ID NOS: 42 and 44, respectively) as primers and DNA from Cytophaga lytica IFO 16020 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 11 and 12, respectively.

EXAMPLE 7

[0075] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 45 and 48 (corresponding to the amino acid sequences of SEQ ID NO: 46 or 47 and SEQ ID NO: 49, respectively) as primers and DNA from Synechococcus sp. PCC 6301 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 13 and 14, respectively.

EXAMPLE 8

[0076] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 53 and 62 (corresponding to the amino acid sequences of SEQ ID NO: 54, 55, 56 or 57 and SEQ ID NO: 63 or 64, respectively) as primers and DNA from Caulobacter crescentus ATCC 15252 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 15 and 16, respectively.

EXAMPLE 9

[0077] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 53 and 58 (corresponding to the amino acid sequences of SEQ ID NO: 54, 55, 56 or 57 and SEQ ID No: 59, respectively) as primers and DNA from Pseudomonas putida ATCC 17484 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 17 and 18, respectively.

EXAMPLE 10

[0078] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 65 and 50 (corresponding to the amino acid sequences of SEQ ID NO: 66, 67 or 68 and SEQ ID NO: 51 or 52, respectively) as primers and DNA from Synechococcus sp. PCC 6301 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 19 and 20, respectively.

EXAMPLE 11

[0079] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 60 and 31 (corresponding to the amino acid sequences of SEQ ID NOS: 61 and 32, respectively) as primers and DNA from Caulobacter crescentus ATCC 15252 strain as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 21 and 22, respectively.

EXAMPLE 12

[0080] A PCR was performed using oligonucleotides represented by the nucleotide sequences shown in SEQ ID NOS: 25 and 43 (corresponding to the amino acid sequences of SEQ ID NOS: 26 and 44, respectively) as primers and DNA from an unidentified strain MBIC 1544 as a template. The PCR amplification conditions were the same as in Example 1. The nucleotide sequence of the amplified DNA fragment and the amino acid sequence deduced therefrom are shown in SEQ ID NOS: 23 and 24, respectively.

[0081] This nucleotide sequence was compared with the nucleotide sequence database possessed by the applicant. As a result, the unidentified strain MBIC 1544 was identified as Cytophaga lytica.

EFFECT OF THE INVENTION

[0082] With the nucleotide sequence of gyr B determined by the pre sent invention, it is possible to classify or identify an unidentified microorganism strain quickly and accurately. Besides, according to the present invention, PCR primers for monitoring a specific microorganism which are needed in risk assessment in various bioprocesses can be designed easily. Also, the present invention enables highly accurate monitoring of changes in mycelial tufts.

1 82 1 1212 DNA Bacteroides vulgatus CDS (1)...(1212) 1 gac aaa ggt tct tac aag gtt tca ggc ggt ctg cac ggt gta ggt gtt 48 Asp Lys Gly Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val 1 5 10 15 tct tgt gtg aac gcc ttg tct act cac atg acc aca cag gta ttc cgc 96 Ser Cys Val Asn Ala Leu Ser Thr His Met Thr Thr Gln Val Phe Arg 20 25 30 ggt ggc aag atc tac cag cag gaa tac agc tgc gga cat cct ttg tat 144 Gly Gly Lys Ile Tyr Gln Gln Glu Tyr Ser Cys Gly His Pro Leu Tyr 35 40 45 tct gta aaa gaa gta gga aca gct gat att acc gga aca aaa cag act 192 Ser Val Lys Glu Val Gly Thr Ala Asp Ile Thr Gly Thr Lys Gln Thr 50 55 60 ttc tgg ccg gat gat acc atc ttc act gtt acc gaa tat aag ttt gac 240 Phe Trp Pro Asp Asp Thr Ile Phe Thr Val Thr Glu Tyr Lys Phe Asp 65 70 75 80 att cta cag gca cgt atg cgt gaa ttg gcc tac ttg aac aaa ggt atc 288 Ile Leu Gln Ala Arg Met Arg Glu Leu Ala Tyr Leu Asn Lys Gly Ile 85 90 95 acc att tca ctg acc gac cgc cgg atc aaa gaa gaa gat ggc agc ttc 336 Thr Ile Ser Leu Thr Asp Arg Arg Ile Lys Glu Glu Asp Gly Ser Phe 100 105 110 aag aaa gaa ata ttc cat tcg gac gaa gga gtg aaa gag ttt gta cgt 384 Lys Lys Glu Ile Phe His Ser Asp Glu Gly Val Lys Glu Phe Val Arg 115 120 125 ttc ctg aac cgt aac aac gaa gcg ctg att aat gat gtc att tat ctg 432 Phe Leu Asn Arg Asn Asn Glu Ala Leu Ile Asn Asp Val Ile Tyr Leu 130 135 140 aat acc gaa aaa aac aat acc ccc att gaa tgt gcc atc atg tac aat 480 Asn Thr Glu Lys Asn Asn Thr Pro Ile Glu Cys Ala Ile Met Tyr Asn 145 150 155 160 aca ggc tat cgt gaa agc ctg cat tcg tat gta aac aat atc aat aca 528 Thr Gly Tyr Arg Glu Ser Leu His Ser Tyr Val Asn Asn Ile Asn Thr 165 170 175 ata gaa ggc ggt aca cac gag gcc ggt ttc cgc agc gca tta acc cgt 576 Ile Glu Gly Gly Thr His Glu Ala Gly Phe Arg Ser Ala Leu Thr Arg 180 185 190 gta ctg aag aaa tat gcg gaa gat acc aaa gca ctg gaa aaa gca aaa 624 Val Leu Lys Lys Tyr Ala Glu Asp Thr Lys Ala Leu Glu Lys Ala Lys 195 200 205 gtc gag att tcg gga gag gac ttc cgc gaa ggc ttg att gcc gtc att 672 Val Glu Ile Ser Gly Glu Asp Phe Arg Glu Gly Leu Ile Ala Val Ile 210 215 220 tca gtg aaa gta gcc gag ccg cag ttc gaa gga cag acc aag acc aag 720 Ser Val Lys Val Ala Glu Pro Gln Phe Glu Gly Gln Thr Lys Thr Lys 225 230 235 240 ctg ggc aac agc gaa gtg agt ggt gcc gtg aac caa gct gta ggc gaa 768 Leu Gly Asn Ser Glu Val Ser Gly Ala Val Asn Gln Ala Val Gly Glu 245 250 255 gcg ctt aca tat tat ctg gaa gaa cat ccg aaa gaa gca aaa cag att 816 Ala Leu Thr Tyr Tyr Leu Glu Glu His Pro Lys Glu Ala Lys Gln Ile 260 265 270 gtt gac aaa gtg atc ctg gct gca aca gcg cgt atc gcc gca cgc aag 864 Val Asp Lys Val Ile Leu Ala Ala Thr Ala Arg Ile Ala Ala Arg Lys 275 280 285 gca cgt gaa tct gtt caa aga aag agt ccg atg ggc ggt ggc gga ctg 912 Ala Arg Glu Ser Val Gln Arg Lys Ser Pro Met Gly Gly Gly Gly Leu 290 295 300 ccg ggc aaa ctg gcc gac tgc tcg agc cgt aat ccg gag gaa tgt gaa 960 Pro Gly Lys Leu Ala Asp Cys Ser Ser Arg Asn Pro Glu Glu Cys Glu 305 310 315 320 cta ttc ctg gtc gag ggt gac tcg gca ggt ggt tct gcc aag caa gga 1008 Leu Phe Leu Val Glu Gly Asp Ser Ala Gly Gly Ser Ala Lys Gln Gly 325 330 335 cgt agc cgt gcc ttc cag gca att cta cct ttg agg ggt aaa atc ctg 1056 Arg Ser Arg Ala Phe Gln Ala Ile Leu Pro Leu Arg Gly Lys Ile Leu 340 345 350 aat gtg gaa aaa gcg atg tgg cac aag gct ttt gaa agc gat gag gtc 1104 Asn Val Glu Lys Ala Met Trp His Lys Ala Phe Glu Ser Asp Glu Val 355 360 365 aat aat atc atc acc gcc ctg ggt gtc cgt ttc ggt gtg gac gga aat 1152 Asn Asn Ile Ile Thr Ala Leu Gly Val Arg Phe Gly Val Asp Gly Asn 370 375 380 gat gac agc aaa aaa gcg aac atc gac aag ctg cgt tat cac aaa gtg 1200 Asp Asp Ser Lys Lys Ala Asn Ile Asp Lys Leu Arg Tyr His Lys Val 385 390 395 400 gtg atc atg acc Val Ile Met Thr 2 404 PRT Bacteroides vulgatus 2 Asp Lys Gly Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val 1 5 10 15 Ser Cys Val Asn Ala Leu Ser Thr His Met Thr Thr Gln Val Phe Arg 20 25 30 Gly Gly Lys Ile Tyr Gln Gln Glu Tyr Ser Cys Gly His Pro Leu Tyr 35 40 45 Ser Val Lys Glu Val Gly Thr Ala Asp Ile Thr Gly Thr Lys Gln Thr 50 55 60 Phe Trp Pro Asp Asp Thr Ile Phe Thr Val Thr Glu Tyr Lys Phe Asp 65 70 75 80 Ile Leu Gln Ala Arg Met Arg Glu Leu Ala Tyr Leu Asn Lys Gly Ile 85 90 95 Thr Ile Ser Leu Thr Asp Arg Arg Ile Lys Glu Glu Asp Gly Ser Phe 100 105 110 Lys Lys Glu Ile Phe His Ser Asp Glu Gly Val Lys Glu Phe Val Arg 115 120 125 Phe Leu Asn Arg Asn Asn Glu Ala Leu Ile Asn Asp Val Ile Tyr Leu 130 135 140 Asn Thr Glu Lys Asn Asn Thr Pro Ile Glu Cys Ala Ile Met Tyr Asn 145 150 155 160 Thr Gly Tyr Arg Glu Ser Leu His Ser Tyr Val Asn Asn Ile Asn Thr 165 170 175 Ile Glu Gly Gly Thr His Glu Ala Gly Phe Arg Ser Ala Leu Thr Arg 180 185 190 Val Leu Lys Lys Tyr Ala Glu Asp Thr Lys Ala Leu Glu Lys Ala Lys 195 200 205 Val Glu Ile Ser Gly Glu Asp Phe Arg Glu Gly Leu Ile Ala Val Ile 210 215 220 Ser Val Lys Val Ala Glu Pro Gln Phe Glu Gly Gln Thr Lys Thr Lys 225 230 235 240 Leu Gly Asn Ser Glu Val Ser Gly Ala Val Asn Gln Ala Val Gly Glu 245 250 255 Ala Leu Thr Tyr Tyr Leu Glu Glu His Pro Lys Glu Ala Lys Gln Ile 260 265 270 Val Asp Lys Val Ile Leu Ala Ala Thr Ala Arg Ile Ala Ala Arg Lys 275 280 285 Ala Arg Glu Ser Val Gln Arg Lys Ser Pro Met Gly Gly Gly Gly Leu 290 295 300 Pro Gly Lys Leu Ala Asp Cys Ser Ser Arg Asn Pro Glu Glu Cys Glu 305 310 315 320 Leu Phe Leu Val Glu Gly Asp Ser Ala Gly Gly Ser Ala Lys Gln Gly 325 330 335 Arg Ser Arg Ala Phe Gln Ala Ile Leu Pro Leu Arg Gly Lys Ile Leu 340 345 350 Asn Val Glu Lys Ala Met Trp His Lys Ala Phe Glu Ser Asp Glu Val 355 360 365 Asn Asn Ile Ile Thr Ala Leu Gly Val Arg Phe Gly Val Asp Gly Asn 370 375 380 Asp Asp Ser Lys Lys Ala Asn Ile Asp Lys Leu Arg Tyr His Lys Val 385 390 395 400 Val Ile Met Thr 3 1263 DNA Mycobacterium simiae CDS (1)...(1263) 3 ggg gag aac agt ggc tac acc gtc agc ggc ggg ttg cac ggg gtc gga 48 Gly Glu Asn Ser Gly Tyr Thr Val Ser Gly Gly Leu His Gly Val Gly 1 5 10 15 gtg tcg gtg gtc aac gcc ctg tcc acc cgc ctg gaa gtc aac gtc aag 96 Val Ser Val Val Asn Ala Leu Ser Thr Arg Leu Glu Val Asn Val Lys 20 25 30 cgt gac ggc tat gag tgg ttc cag tac tac gac cgg gcg gtg ccc ggc 144 Arg Asp Gly Tyr Glu Trp Phe Gln Tyr Tyr Asp Arg Ala Val Pro Gly 35 40 45 acc ctc aag caa ggc gag gcg acc aag aag acc ggc acc acg atc cgg 192 Thr Leu Lys Gln Gly Glu Ala Thr Lys Lys Thr Gly Thr Thr Ile Arg 50 55 60 ttc tgg gcc gat cct gag atc ttc gaa acc acc cag tac gac ttc gag 240 Phe Trp Ala Asp Pro Glu Ile Phe Glu Thr Thr Gln Tyr Asp Phe Glu 65 70 75 80 acg gtg gcg cgc cgg ttg cag gaa atg gcg ttc ctc aac aag ggc ctg 288 Thr Val Ala Arg Arg Leu Gln Glu Met Ala Phe Leu Asn Lys Gly Leu 85 90 95 acc atc aac ctc acc gac gaa cgt gtc gag cag gac gag gtg gtc gat 336 Thr Ile Asn Leu Thr Asp Glu Arg Val Glu Gln Asp Glu Val Val Asp 100 105 110 gag gtg gtt agc gac acc gcc gag gcg ccg aag tca gcc gag gag cag 384 Glu Val Val Ser Asp Thr Ala Glu Ala Pro Lys Ser Ala Glu Glu Gln 115 120 125 gcg gcc gaa tcg gcc aag ccg cac aag gtc aag cac cgc acg ttc cac 432 Ala Ala Glu Ser Ala Lys Pro His Lys Val Lys His Arg Thr Phe His 130 135 140 tac ccg ggt ggg ttg gtg gat ttc gtc aag cac atc aat cgc acc aaa 480 Tyr Pro Gly Gly Leu Val Asp Phe Val Lys His Ile Asn Arg Thr Lys 145 150 155 160 aac ccg atc cag cag agc gtc atc gac ttc gac ggc aaa gga acc ggg 528 Asn Pro Ile Gln Gln Ser Val Ile Asp Phe Asp Gly Lys Gly Thr Gly 165 170 175 cac gaa gtc gag atc gcg atg cag tgg aac ggt ggt tat tcg gag tcg 576 His Glu Val Glu Ile Ala Met Gln Trp Asn Gly Gly Tyr Ser Glu Ser 180 185 190 gtg cac acc ttc gcc aac acc atc aac acc cat gag ggc ggc acc cac 624 Val His Thr Phe Ala Asn Thr Ile Asn Thr His Glu Gly Gly Thr His 195 200 205 gag gag ggc ttc cgc agc gcg ctg acc tcg gtg gtg aac aag tac gcc 672 Glu Glu Gly Phe Arg Ser Ala Leu Thr Ser Val Val Asn Lys Tyr Ala 210 215 220 aaa gac aag aag ctg ctc aag gac aag gat ccc aac ctc acc ggc gac 720 Lys Asp Lys Lys Leu Leu Lys Asp Lys Asp Pro Asn Leu Thr Gly Asp 225 230 235 240 gac atc cga gaa ggg ctg gcc gcg gtg atc tcc gtg aag gtc gcc gag 768 Asp Ile Arg Glu Gly Leu Ala Ala Val Ile Ser Val Lys Val Ala Glu 245 250 255 ccg cag ttc gag ggc cag act aag acg aaa ctc ggc aac acc gag gtc 816 Pro Gln Phe Glu Gly Gln Thr Lys Thr Lys Leu Gly Asn Thr Glu Val 260 265 270 aag tcg ttt gtc cag aaa gtc tgt aac gaa caa ctc act cac tgg ttc 864 Lys Ser Phe Val Gln Lys Val Cys Asn Glu Gln Leu Thr His Trp Phe 275 280 285 gag gcg aac ccg tcg gaa gct aaa acc gtt gta aac aag gcg gtt tcg 912 Glu Ala Asn Pro Ser Glu Ala Lys Thr Val Val Asn Lys Ala Val Ser 290 295 300 tcg gcc cag gcc cgc att gcg gcg cgt aag gcg cgg gag ttg gtg cgg 960 Ser Ala Gln Ala Arg Ile Ala Ala Arg Lys Ala Arg Glu Leu Val Arg 305 310 315 320 cgt aag agt gct acg gat ttg ggt ggg ttg ccg ggc aag ttg gct gat 1008 Arg Lys Ser Ala Thr Asp Leu Gly Gly Leu Pro Gly Lys Leu Ala Asp 325 330 335 tgc cgc tcg acg gat ccg cgg aag tct gag ctg tat gtg gtg gaa ggt 1056 Cys Arg Ser Thr Asp Pro Arg Lys Ser Glu Leu Tyr Val Val Glu Gly 340 345 350 gat tcc gcg ggt ggg tcg gcg aaa agt ggg cgt gat tcg atg ttc cag 1104 Asp Ser Ala Gly Gly Ser Ala Lys Ser Gly Arg Asp Ser Met Phe Gln 355 360 365 gcg atc ttg ccg ctg cgc ggc aag atc atc aac gtc gaa aag gcc cgc 1152 Ala Ile Leu Pro Leu Arg Gly Lys Ile Ile Asn Val Glu Lys Ala Arg 370 375 380 atc gat cgg gtg ctg aaa aac acc gaa gtc cag gcc atc atc acc gcg 1200 Ile Asp Arg Val Leu Lys Asn Thr Glu Val Gln Ala Ile Ile Thr Ala 385 390 395 400 ctg ggc acc ggc atc cac gac gaa ttc gac atc acc aaa ctg cgt tac 1248 Leu Gly Thr Gly Ile His Asp Glu Phe Asp Ile Thr Lys Leu Arg Tyr 405 410 415 cac aag atc gtg ttg 1263 His Lys Ile Val Leu 420 4 421 PRT Mycobacterium simiae 4 Gly Glu Asn Ser Gly Tyr Thr Val Ser Gly Gly Leu His Gly Val Gly 1 5 10 15 Val Ser Val Val Asn Ala Leu Ser Thr Arg Leu Glu Val Asn Val Lys 20 25 30 Arg Asp Gly Tyr Glu Trp Phe Gln Tyr Tyr Asp Arg Ala Val Pro Gly 35 40 45 Thr Leu Lys Gln Gly Glu Ala Thr Lys Lys Thr Gly Thr Thr Ile Arg 50 55 60 Phe Trp Ala Asp Pro Glu Ile Phe Glu Thr Thr Gln Tyr Asp Phe Glu 65 70 75 80 Thr Val Ala Arg Arg Leu Gln Glu Met Ala Phe Leu Asn Lys Gly Leu 85 90 95 Thr Ile Asn Leu Thr Asp Glu Arg Val Glu Gln Asp Glu Val Val Asp 100 105 110 Glu Val Val Ser Asp Thr Ala Glu Ala Pro Lys Ser Ala Glu Glu Gln 115 120 125 Ala Ala Glu Ser Ala Lys Pro His Lys Val Lys His Arg Thr Phe His 130 135 140 Tyr Pro Gly Gly Leu Val Asp Phe Val Lys His Ile Asn Arg Thr Lys 145 150 155 160 Asn Pro Ile Gln Gln Ser Val Ile Asp Phe Asp Gly Lys Gly Thr Gly 165 170 175 His Glu Val Glu Ile Ala Met Gln Trp Asn Gly Gly Tyr Ser Glu Ser 180 185 190 Val His Thr Phe Ala Asn Thr Ile Asn Thr His Glu Gly Gly Thr His 195 200 205 Glu Glu Gly Phe Arg Ser Ala Leu Thr Ser Val Val Asn Lys Tyr Ala 210 215 220 Lys Asp Lys Lys Leu Leu Lys Asp Lys Asp Pro Asn Leu Thr Gly Asp 225 230 235 240 Asp Ile Arg Glu Gly Leu Ala Ala Val Ile Ser Val Lys Val Ala Glu 245 250 255 Pro Gln Phe Glu Gly Gln Thr Lys Thr Lys Leu Gly Asn Thr Glu Val 260 265 270 Lys Ser Phe Val Gln Lys Val Cys Asn Glu Gln Leu Thr His Trp Phe 275 280 285 Glu Ala Asn Pro Ser Glu Ala Lys Thr Val Val Asn Lys Ala Val Ser 290 295 300 Ser Ala Gln Ala Arg Ile Ala Ala Arg Lys Ala Arg Glu Leu Val Arg 305 310 315 320 Arg Lys Ser Ala Thr Asp Leu Gly Gly Leu Pro Gly Lys Leu Ala Asp 325 330 335 Cys Arg Ser Thr Asp Pro Arg Lys Ser Glu Leu Tyr Val Val Glu Gly 340 345 350 Asp Ser Ala Gly Gly Ser Ala Lys Ser Gly Arg Asp Ser Met Phe Gln 355 360 365 Ala Ile Leu Pro Leu Arg Gly Lys Ile Ile Asn Val Glu Lys Ala Arg 370 375 380 Ile Asp Arg Val Leu Lys Asn Thr Glu Val Gln Ala Ile Ile Thr Ala 385 390 395 400 Leu Gly Thr Gly Ile His Asp Glu Phe Asp Ile Thr Lys Leu Arg Tyr 405 410 415 His Lys Ile Val Leu 420 5 660 DNA Chitinophaga pinensis CDS (1)...(660) 5 gta gca ggc ttc cgc cgt gcg ata acc cgt atc ttc aag agc tat ggt 48 Val Ala Gly Phe Arg Arg Ala Ile Thr Arg Ile Phe Lys Ser Tyr Gly 1 5 10 15 gat aag aac aaa atg ttc gaa aaa acc aag atc gaa gta aca ggt gat 96 Asp Lys Asn Lys Met Phe Glu Lys Thr Lys Ile Glu Val Thr Gly Asp 20 25 30 gac ttc cgt gaa ggt ctg agc gct atc atc agc gta aaa gta cct gaa 144 Asp Phe Arg Glu Gly Leu Ser Ala Ile Ile Ser Val Lys Val Pro Glu 35 40 45 cca cag ttc gaa ggc cag acc aaa acc aaa ctc ggt aac tcc gat gta 192 Pro Gln Phe Glu Gly Gln Thr Lys Thr Lys Leu Gly Asn Ser Asp Val 50 55 60 atg ggg gtt gtg gac agt tcc gta gca gcc gta ctg gat gcc tac ctg 240 Met Gly Val Val Asp Ser Ser Val Ala Ala Val Leu Asp Ala Tyr Leu 65 70 75 80 gaa gaa cat ccc cgc gaa gcc aag atc att atc aat aaa gtg gta ctg 288 Glu Glu His Pro Arg Glu Ala Lys Ile Ile Ile Asn Lys Val Val Leu 85 90 95 gca gca cag gcg cgt gaa gca gcc cgt aaa gca cgc cag atg gta cag 336 Ala Ala Gln Ala Arg Glu Ala Ala Arg Lys Ala Arg Gln Met Val Gln 100 105 110 cgt aag agc gta ctg agt gga agc ggc ttg cct ggt aaa ctg gct gac 384 Arg Lys Ser Val Leu Ser Gly Ser Gly Leu Pro Gly Lys Leu Ala Asp 115 120 125 tgc tct gaa aat gat cct gaa aaa tgt gaa ctg tac ctg gta gag ggt 432 Cys Ser Glu Asn Asp Pro Glu Lys Cys Glu Leu Tyr Leu Val Glu Gly 130 135 140 gac tcc gca ggt ggt acg gct aaa caa gga cgt aac cgt agc ttc cag 480 Asp Ser Ala Gly Gly Thr Ala Lys Gln Gly Arg Asn Arg Ser Phe Gln 145 150 155 160 gcg atc ctg ccg ctc agg ggt aaa atc ctg aac gtg gag aaa gcc atg 528 Ala Ile Leu Pro Leu Arg Gly Lys Ile Leu Asn Val Glu Lys Ala Met 165 170 175 gag cat aag ata tat gag aat gag gag att aaa aac atc ttc acc gca 576 Glu His Lys Ile Tyr Glu Asn Glu Glu Ile Lys Asn Ile Phe Thr Ala 180 185 190 ctt ggt gta acc atc ggt acg gaa gaa gat gac aaa gcc ctc aac ctc 624 Leu Gly Val Thr Ile Gly Thr Glu Glu Asp Asp Lys Ala Leu Asn Leu 195 200 205 tcc aaa ctg cgc tat cac aaa ctg atc atc atg acg 660 Ser Lys Leu Arg Tyr His Lys Leu Ile Ile Met Thr 210 215 220 6 220 PRT Chitinophaga pinensis 6 Val Ala Gly Phe Arg Arg Ala Ile Thr Arg Ile Phe Lys Ser Tyr Gly 1 5 10 15 Asp Lys Asn Lys Met Phe Glu Lys Thr Lys Ile Glu Val Thr Gly Asp 20 25 30 Asp Phe Arg Glu Gly Leu Ser Ala Ile Ile Ser Val Lys Val Pro Glu 35 40 45 Pro Gln Phe Glu Gly Gln Thr Lys Thr Lys Leu Gly Asn Ser Asp Val 50 55 60 Met Gly Val Val Asp Ser Ser Val Ala Ala Val Leu Asp Ala Tyr Leu 65 70 75 80 Glu Glu His Pro Arg Glu Ala Lys Ile Ile Ile Asn Lys Val Val Leu 85 90 95 Ala Ala Gln Ala Arg Glu Ala Ala Arg Lys Ala Arg Gln Met Val Gln 100 105 110 Arg Lys Ser Val Leu Ser Gly Ser Gly Leu Pro Gly Lys Leu Ala Asp 115 120 125 Cys Ser Glu Asn Asp Pro Glu Lys Cys Glu Leu Tyr Leu Val Glu Gly 130 135 140 Asp Ser Ala Gly Gly Thr Ala Lys Gln Gly Arg Asn Arg Ser Phe Gln 145 150 155 160 Ala Ile Leu Pro Leu Arg Gly Lys Ile Leu Asn Val Glu Lys Ala Met 165 170 175 Glu His Lys Ile Tyr Glu Asn Glu Glu Ile Lys Asn Ile Phe Thr Ala 180 185 190 Leu Gly Val Thr Ile Gly Thr Glu Glu Asp Asp Lys Ala Leu Asn Leu 195 200 205 Ser Lys Leu Arg Tyr His Lys Leu Ile Ile Met Thr 210 215 220 7 537 DNA Flavobacterium aquatile CDS (1)...(537) 7 gat aaa gat tct tat aaa gtt tcg ggt gga ctt cac gga gtt ggt gtt 48 Asp Lys Asp Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val 1 5 10 15 tct tgc gtt aat gca ctt tct gat aac cta aaa gca acc gtt ttt aga 96 Ser Cys Val Asn Ala Leu Ser Asp Asn Leu Lys Ala Thr Val Phe Arg 20 25 30 gac gga aaa gtg tac gag caa gaa tat gaa aaa ggt aaa gca atg tat 144 Asp Gly Lys Val Tyr Glu Gln Glu Tyr Glu Lys Gly Lys Ala Met Tyr 35 40 45 ccg gtt aag caa gtt ggt gaa aca aca aag cga gga aca atg gtt act 192 Pro Val Lys Gln Val Gly Glu Thr Thr Lys Arg Gly Thr Met Val Thr 50 55 60 ttt cat cct gat aaa acc att ttt act caa aca att gag tat tct tat 240 Phe His Pro Asp Lys Thr Ile Phe Thr Gln Thr Ile Glu Tyr Ser Tyr 65 70 75 80 gat aca ctt gca gca cgt atg cgt gaa tta tct ttc ctg aat aaa gga 288 Asp Thr Leu Ala Ala Arg Met Arg Glu Leu Ser Phe Leu Asn Lys Gly 85 90 95 att aca atc aca ctt aca gat aaa aga cat act aaa gac aac ggc gat 336 Ile Thr Ile Thr Leu Thr Asp Lys Arg His Thr Lys Asp Asn Gly Asp 100 105 110 ttt gaa ggt gaa gtt ttt cat tct aaa gaa ggg ctt aaa gaa ttc gtt 384 Phe Glu Gly Glu Val Phe His Ser Lys Glu Gly Leu Lys Glu Phe Val 115 120 125 cga ttt tta gat gct ggt aga gaa cca att att tct cac gta ata agc 432 Arg Phe Leu Asp Ala Gly Arg Glu Pro Ile Ile Ser His Val Ile Ser 130 135 140 atg gag cac gaa aaa gga gaa gtt cct gtt gag gtt gct ctt gtt tac 480 Met Glu His Glu Lys Gly Glu Val Pro Val Glu Val Ala Leu Val Tyr 145 150 155 160 aat aca agt tac tcc gaa aat att ttc tct tac gta aat aat att aac 528 Asn Thr Ser Tyr Ser Glu Asn Ile Phe Ser Tyr Val Asn Asn Ile Asn 165 170 175 acg cac gaa 537 Thr His Glu 8 179 PRT Flavobacterium aquatile 8 Asp Lys Asp Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val 1 5 10 15 Ser Cys Val Asn Ala Leu Ser Asp Asn Leu Lys Ala Thr Val Phe Arg 20 25 30 Asp Gly Lys Val Tyr Glu Gln Glu Tyr Glu Lys Gly Lys Ala Met Tyr 35 40 45 Pro Val Lys Gln Val Gly Glu Thr Thr Lys Arg Gly Thr Met Val Thr 50 55 60 Phe His Pro Asp Lys Thr Ile Phe Thr Gln Thr Ile Glu Tyr Ser Tyr 65 70 75 80 Asp Thr Leu Ala Ala Arg Met Arg Glu Leu Ser Phe Leu Asn Lys Gly 85 90 95 Ile Thr Ile Thr Leu Thr Asp Lys Arg His Thr Lys Asp Asn Gly Asp 100 105 110 Phe Glu Gly Glu Val Phe His Ser Lys Glu Gly Leu Lys Glu Phe Val 115 120 125 Arg Phe Leu Asp Ala Gly Arg Glu Pro Ile Ile Ser His Val Ile Ser 130 135 140 Met Glu His Glu Lys Gly Glu Val Pro Val Glu Val Ala Leu Val Tyr 145 150 155 160 Asn Thr Ser Tyr Ser Glu Asn Ile Phe Ser Tyr Val Asn Asn Ile Asn 165 170 175 Thr His Glu 9 783 DNA Mycobacterium asiaticum CDS (1)...(783) 9 ggc gag aac agc ggc tac acc gtc agc ggt ggg ttg cac gga gtg ggc 48 Gly Glu Asn Ser Gly Tyr Thr Val Ser Gly Gly Leu His Gly Val Gly 1 5 10 15 gtg tcg gtg gtc aac gcg ctg tcc acc cgc ctg gag gtc acc atc aag 96 Val Ser Val Val Asn Ala Leu Ser Thr Arg Leu Glu Val Thr Ile Lys 20 25 30 cgc gac ggg cac gag tgg ttt cag tac tac gac cgc gcc gtg ccc gga 144 Arg Asp Gly His Glu Trp Phe Gln Tyr Tyr Asp Arg Ala Val Pro Gly 35 40 45 acc ctc aag cag ggc gag gcc acc aag aag acc gga acc acg atc agg 192 Thr Leu Lys Gln Gly Glu Ala Thr Lys Lys Thr Gly Thr Thr Ile Arg 50 55 60 ttc tgg gcg gac ccc gaa atc ttc gaa acc aca cag tac gac ttc gag 240 Phe Trp Ala Asp Pro Glu Ile Phe Glu Thr Thr Gln Tyr Asp Phe Glu 65 70 75 80 acc gtg gcg cgg cgg ctg cag gag atg gcc ttc ctc aac aag ggc ctc 288 Thr Val Ala Arg Arg Leu Gln Glu Met Ala Phe Leu Asn Lys Gly Leu 85 90 95 acc atc aac ctc acc gac gaa cga gtg gag cag gac gag gtc gtc gac 336 Thr Ile Asn Leu Thr Asp Glu Arg Val Glu Gln Asp Glu Val Val Asp 100 105 110 gag gtc gtc agc gac acc gcc gag gca ccg aag tcc gcc gaa gag aag 384 Glu Val Val Ser Asp Thr Ala Glu Ala Pro Lys Ser Ala Glu Glu Lys 115 120 125 gcc gcg gaa tcg act gcg cca cac aag gtc aag cac cgc acc ttc cac 432 Ala Ala Glu Ser Thr Ala Pro His Lys Val Lys His Arg Thr Phe His 130 135 140 tac ccc ggc ggt ctg gtc gac ttc gtc aag cac atc aac cgc acc aag 480 Tyr Pro Gly Gly Leu Val Asp Phe Val Lys His Ile Asn Arg Thr Lys 145 150 155 160 agc ccg atc cag cag agc gtc atc gat ttc gac ggc aag ggc acc ggc 528 Ser Pro Ile Gln Gln Ser Val Ile Asp Phe Asp Gly Lys Gly Thr Gly 165 170 175 cac gag gtc gag atc gcc atg cag tgg aac ggc ggc tac tcg gag tcc 576 His Glu Val Glu Ile Ala Met Gln Trp Asn Gly Gly Tyr Ser Glu Ser 180 185 190 gtc cac acc ttc gcc aac acc atc aac acg cac gag ggc ggc acc cac 624 Val His Thr Phe Ala Asn Thr Ile Asn Thr His Glu Gly Gly Thr His 195 200 205 gag gag ggc ttc cgc agc gcg ctg acg tcg gtg gtg aac aag tac gcc 672 Glu Glu Gly Phe Arg Ser Ala Leu Thr Ser Val Val Asn Lys Tyr Ala 210 215 220 aaa gac aag aaa ctg ctg aag gac aaa gat ccc aac ctc acc ggt gac 720 Lys Asp Lys Lys Leu Leu Lys Asp Lys Asp Pro Asn Leu Thr Gly Asp 225 230 235 240 gac atc cgt gag ggc ttg gcc gcg gtc atc tcg gtg aag gtc gcc gag 768 Asp Ile Arg Glu Gly Leu Ala Ala Val Ile Ser Val Lys Val Ala Glu 245 250 255 cca cag ttc gaa ggc 783 Pro Gln Phe Glu Gly 260 10 261 PRT Mycobacterium asiaticum 10 Gly Glu Asn Ser Gly Tyr Thr Val Ser Gly Gly Leu His Gly Val Gly 1 5 10 15 Val Ser Val Val Asn Ala Leu Ser Thr Arg Leu Glu Val Thr Ile Lys 20 25 30 Arg Asp Gly His Glu Trp Phe Gln Tyr Tyr Asp Arg Ala Val Pro Gly 35 40 45 Thr Leu Lys Gln Gly Glu Ala Thr Lys Lys Thr Gly Thr Thr Ile Arg 50 55 60 Phe Trp Ala Asp Pro Glu Ile Phe Glu Thr Thr Gln Tyr Asp Phe Glu 65 70 75 80 Thr Val Ala Arg Arg Leu Gln Glu Met Ala Phe Leu Asn Lys Gly Leu 85 90 95 Thr Ile Asn Leu Thr Asp Glu Arg Val Glu Gln Asp Glu Val Val Asp 100 105 110 Glu Val Val Ser Asp Thr Ala Glu Ala Pro Lys Ser Ala Glu Glu Lys 115 120 125 Ala Ala Glu Ser Thr Ala Pro His Lys Val Lys His Arg Thr Phe His 130 135 140 Tyr Pro Gly Gly Leu Val Asp Phe Val Lys His Ile Asn Arg Thr Lys 145 150 155 160 Ser Pro Ile Gln Gln Ser Val Ile Asp Phe Asp Gly Lys Gly Thr Gly 165 170 175 His Glu Val Glu Ile Ala Met Gln Trp Asn Gly Gly Tyr Ser Glu Ser 180 185 190 Val His Thr Phe Ala Asn Thr Ile Asn Thr His Glu Gly Gly Thr His 195 200 205 Glu Glu Gly Phe Arg Ser Ala Leu Thr Ser Val Val Asn Lys Tyr Ala 210 215 220 Lys Asp Lys Lys Leu Leu Lys Asp Lys Asp Pro Asn Leu Thr Gly Asp 225 230 235 240 Asp Ile Arg Glu Gly Leu Ala Ala Val Ile Ser Val Lys Val Ala Glu 245 250 255 Pro Gln Phe Glu Gly 260 11 195 DNA Cytophaga lytica CDS (1)...(195) 11 agc cac att gaa act tta att ctt aca ttc ttc ttc cgt ttt atg cga 48 Ser His Ile Glu Thr Leu Ile Leu Thr Phe Phe Phe Arg Phe Met Arg 1 5 10 15 gaa cta ata gaa ggc gga cac gtt tac ata gca aca cca cct tta tat 96 Glu Leu Ile Glu Gly Gly His Val Tyr Ile Ala Thr Pro Pro Leu Tyr 20 25 30 tta gtt aaa aaa gga act aaa aag cgt tat gct tgg aat gat aaa gaa 144 Leu Val Lys Lys Gly Thr Lys Lys Arg Tyr Ala Trp Asn Asp Lys Glu 35 40 45 cga gat gaa ata gca gat agc ttt aat ggt agt gta ggt atc caa aga 192 Arg Asp Glu Ile Ala Asp Ser Phe Asn Gly Ser Val Gly Ile Gln Arg 50 55 60 tat 195 Tyr 65 12 65 PRT Cytophaga lytica 12 Ser His Ile Glu Thr Leu Ile Leu Thr Phe Phe Phe Arg Phe Met Arg 1 5 10 15 Glu Leu Ile Glu Gly Gly His Val Tyr Ile Ala Thr Pro Pro Leu Tyr 20 25 30 Leu Val Lys Lys Gly Thr Lys Lys Arg Tyr Ala Trp Asn Asp Lys Glu 35 40 45 Arg Asp Glu Ile Ala Asp Ser Phe Asn Gly Ser Val Gly Ile Gln Arg 50 55 60 Tyr 65 13 1170 DNA Synechococcus sp. CDS (1)...(1170) 13 gtg gtg gac aac gcc gtc gac aaa gcc ttg gcg ggc tac tgc aat acc 48 Val Val Asp Asn Ala Val Asp Lys Ala Leu Ala Gly Tyr Cys Asn Thr 1 5 10 15 att gat gtt cgt ctg ctc aaa gac ggc tcc tgc caa gtc acc gat aac 96 Ile Asp Val Arg Leu Leu Lys Asp Gly Ser Cys Gln Val Thr Asp Asn 20 25 30 ggt cgc ggc att ccc aca gat att cac ccc caa acc ggg aag tct gct 144 Gly Arg Gly Ile Pro Thr Asp Ile His Pro Gln Thr Gly Lys Ser Ala 35 40 45 ctc gaa acc gtg ctg acg att ctg cac gcg ggc ggc aag ttt ggc ggt 192 Leu Glu Thr Val Leu Thr Ile Leu His Ala Gly Gly Lys Phe Gly Gly 50 55 60 ggc ggt tat aag gtg tcg ggg ggt ctg cac ggc gtc ggt gtg tct gtc 240 Gly Gly Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val Ser Val 65 70 75 80 gtc aac gcc ctc tca gaa tat gtc gaa gtc acc gtg tgg cgg gaa ggc 288 Val Asn Ala Leu Ser Glu Tyr Val Glu Val Thr Val Trp Arg Glu Gly 85 90 95 aaa acc cac caa cag cgc ttt gaa cag ggc aac ccg atc ggg gag ttg 336 Lys Thr His Gln Gln Arg Phe Glu Gln Gly Asn Pro Ile Gly Glu Leu 100 105 110 caa gtt gcc ccg gat gcc gac gat cgc cgc ggg aca caa gtt cgt ttc 384 Gln Val Ala Pro Asp Ala Asp Asp Arg Arg Gly Thr Gln Val Arg Phe 115 120 125 aaa cca gac gcc acg atc ttt tct gaa aca acc gag ttc gat tac ggc 432 Lys Pro Asp Ala Thr Ile Phe Ser Glu Thr Thr Glu Phe Asp Tyr Gly 130 135 140 acc cta gca agc cga ttg aag gag cta gcc tat ctg aat gcg ggc gtc 480 Thr Leu Ala Ser Arg Leu Lys Glu Leu Ala Tyr Leu Asn Ala Gly Val 145 150 155 160 cgc atc gac ttt acc gat gag cgg ctg cag ctc acc aag aat cac gag 528 Arg Ile Asp Phe Thr Asp Glu Arg Leu Gln Leu Thr Lys Asn His Glu 165 170 175 ccc cat caa gaa acc tat tac ttt gaa ggc ggt att cgc gaa tac gtc 576 Pro His Gln Glu Thr Tyr Tyr Phe Glu Gly Gly Ile Arg Glu Tyr Val 180 185 190 gcc tac atg aat acc gat aaa cag gcg ctg cac tca gag att atc ttt 624 Ala Tyr Met Asn Thr Asp Lys Gln Ala Leu His Ser Glu Ile Ile Phe 195 200 205 gtg caa tcc gaa aaa gat ggc gtc caa gtt gaa gct gca ttg caa tgg 672 Val Gln Ser Glu Lys Asp Gly Val Gln Val Glu Ala Ala Leu Gln Trp 210 215 220 tgc gtt gac gcc tac agc gac aac att ctg ggc ttt gcc aac aac atc 720 Cys Val Asp Ala Tyr Ser Asp Asn Ile Leu Gly Phe Ala Asn Asn Ile 225 230 235 240 cgc acg att gac ggc ggc acc cat att gag ggg ctc aaa act gtt ctg 768 Arg Thr Ile Asp Gly Gly Thr His Ile Glu Gly Leu Lys Thr Val Leu 245 250 255 acg cgg acg atg aac acg atc gcc cgc aaa cgg aat aaa cgc aag gat 816 Thr Arg Thr Met Asn Thr Ile Ala Arg Lys Arg Asn Lys Arg Lys Asp 260 265 270 gcc gac aat aac ctg tcg ggc gag aat att cgc gaa ggg tta aca gcg 864 Ala Asp Asn Asn Leu Ser Gly Glu Asn Ile Arg Glu Gly Leu Thr Ala 275 280 285 atc gtt tcg gtc aaa gtt ccg gat ccg gaa ttt gaa ggg caa acc aaa 912 Ile Val Ser Val Lys Val Pro Asp Pro Glu Phe Glu Gly Gln Thr Lys 290 295 300 aca aag ctc ggc aat acc gaa gtt cgc ggc atc gtc gat acg ctc gtg 960 Thr Lys Leu Gly Asn Thr Glu Val Arg Gly Ile Val Asp Thr Leu Val 305 310 315 320 ggc gaa acg ttg acg gaa tat ctg gaa ttc cat ccc agc gtt gcc gat 1008 Gly Glu Thr Leu Thr Glu Tyr Leu Glu Phe His Pro Ser Val Ala Asp 325 330 335 ttg atc ctc gaa aaa gcg att caa gcc ttt aat gcg gct gag gca gcg 1056 Leu Ile Leu Glu Lys Ala Ile Gln Ala Phe Asn Ala Ala Glu Ala Ala 340 345 350 cga cgg gca cgg gaa ttg gtg cgt cgc aaa tca gtg ctg gaa tct tcg 1104 Arg Arg Ala Arg Glu Leu Val Arg Arg Lys Ser Val Leu Glu Ser Ser 355 360 365 aca ttg ccc ggt aaa tta gca gac tgt tcc agt cgc gat ccc ggt gaa 1152 Thr Leu Pro Gly Lys Leu Ala Asp Cys Ser Ser Arg Asp Pro Gly Glu 370 375 380 tct gaa atc ttc atc gtg 1170 Ser Glu Ile Phe Ile Val 385 390 14 390 PRT Synechococcus sp. 14 Val Val Asp Asn Ala Val Asp Lys Ala Leu Ala Gly Tyr Cys Asn Thr 1 5 10 15 Ile Asp Val Arg Leu Leu Lys Asp Gly Ser Cys Gln Val Thr Asp Asn 20 25 30 Gly Arg Gly Ile Pro Thr Asp Ile His Pro Gln Thr Gly Lys Ser Ala 35 40 45 Leu Glu Thr Val Leu Thr Ile Leu His Ala Gly Gly Lys Phe Gly Gly 50 55 60 Gly Gly Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val Ser Val 65 70 75 80 Val Asn Ala Leu Ser Glu Tyr Val Glu Val Thr Val Trp Arg Glu Gly 85 90 95 Lys Thr His Gln Gln Arg Phe Glu Gln Gly Asn Pro Ile Gly Glu Leu 100 105 110 Gln Val Ala Pro Asp Ala Asp Asp Arg Arg Gly Thr Gln Val Arg Phe 115 120 125 Lys Pro Asp Ala Thr Ile Phe Ser Glu Thr Thr Glu Phe Asp Tyr Gly 130 135 140 Thr Leu Ala Ser Arg Leu Lys Glu Leu Ala Tyr Leu Asn Ala Gly Val 145 150 155 160 Arg Ile Asp Phe Thr Asp Glu Arg Leu Gln Leu Thr Lys Asn His Glu 165 170 175 Pro His Gln Glu Thr Tyr Tyr Phe Glu Gly Gly Ile Arg Glu Tyr Val 180 185 190 Ala Tyr Met Asn Thr Asp Lys Gln Ala Leu His Ser Glu Ile Ile Phe 195 200 205 Val Gln Ser Glu Lys Asp Gly Val Gln Val Glu Ala Ala Leu Gln Trp 210 215 220 Cys Val Asp Ala Tyr Ser Asp Asn Ile Leu Gly Phe Ala Asn Asn Ile 225 230 235 240 Arg Thr Ile Asp Gly Gly Thr His Ile Glu Gly Leu Lys Thr Val Leu 245 250 255 Thr Arg Thr Met Asn Thr Ile Ala Arg Lys Arg Asn Lys Arg Lys Asp 260 265 270 Ala Asp Asn Asn Leu Ser Gly Glu Asn Ile Arg Glu Gly Leu Thr Ala 275 280 285 Ile Val Ser Val Lys Val Pro Asp Pro Glu Phe Glu Gly Gln Thr Lys 290 295 300 Thr Lys Leu Gly Asn Thr Glu Val Arg Gly Ile Val Asp Thr Leu Val 305 310 315 320 Gly Glu Thr Leu Thr Glu Tyr Leu Glu Phe His Pro Ser Val Ala Asp 325 330 335 Leu Ile Leu Glu Lys Ala Ile Gln Ala Phe Asn Ala Ala Glu Ala Ala 340 345 350 Arg Arg Ala Arg Glu Leu Val Arg Arg Lys Ser Val Leu Glu Ser Ser 355 360 365 Thr Leu Pro Gly Lys Leu Ala Asp Cys Ser Ser Arg Asp Pro Gly Glu 370 375 380 Ser Glu Ile Phe Ile Val 385 390 15 696 DNA Caulobacter crescentus CDS (1)...(696) 15 cag aac agc tac aag gtc tcg ggc ggt ctg cac ggc gtg ggc gtc tcg 48 Gln Asn Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val Ser 1 5 10 15 gtc gtg aac gcc ctg tcg gat tgg ctg gag ctg ctg atc cac cgc aac 96 Val Val Asn Ala Leu Ser Asp Trp Leu Glu Leu Leu Ile His Arg Asn 20 25 30 ggc aag gtc cac cag atg cgc ttc gag cgc ggc gac gcg gtc acc tcg 144 Gly Lys Val His Gln Met Arg Phe Glu Arg Gly Asp Ala Val Thr Ser 35 40 45 ctg aag gtc acc ggc gac tcg ccc gtg cgg acc gag ggc ccc aag gcc 192 Leu Lys Val Thr Gly Asp Ser Pro Val Arg Thr Glu Gly Pro Lys Ala 50 55 60 ggc gag acc ctg acc ggt acg gaa gtt acg ttc ttt ccg tcg aag gac 240 Gly Glu Thr Leu Thr Gly Thr Glu Val Thr Phe Phe Pro Ser Lys Asp 65 70 75 80 acc ttc gcc ttc atc gaa ttc gac cgg aag acg ctg gag cac cgc ctg 288 Thr Phe Ala Phe Ile Glu Phe Asp Arg Lys Thr Leu Glu His Arg Leu 85 90 95 cgc gag ctg gcc ttc ctg aac tcg ggc gtg acg atc tgg ttc aag gac 336 Arg Glu Leu Ala Phe Leu Asn Ser Gly Val Thr Ile Trp Phe Lys Asp 100 105 110 cat cgc gac gtc gag ccg tgg gaa gag aag ctg ttc tac gag ggc ggc 384 His Arg Asp Val Glu Pro Trp Glu Glu Lys Leu Phe Tyr Glu Gly Gly 115 120 125 atc gag gcc ttc gtg cgc cac ctc gac aag gcc aag acg ccg ctg ctg 432 Ile Glu Ala Phe Val Arg His Leu Asp Lys Ala Lys Thr Pro Leu Leu 130 135 140 aag gcc ccg atc gcc gtc aag ggc gtc aag gac aag gtc gag atc gac 480 Lys Ala Pro Ile Ala Val Lys Gly Val Lys Asp Lys Val Glu Ile Asp 145 150 155 160 ctg gcc ctg tgg tgg aac gac agc tac cac gag cag atg ctg tgc ttc 528 Leu Ala Leu Trp Trp Asn Asp Ser Tyr His Glu Gln Met Leu Cys Phe 165 170 175 acc aac aac atc ccg cag cgg gat ggc ggc acg cac ctg tcg gcc ttt 576 Thr Asn Asn Ile Pro Gln Arg Asp Gly Gly Thr His Leu Ser Ala Phe 180 185 190 cgc gcg gcc ctg acc cgg atc atc acc agc tac gcc gag agc tcc ggc 624 Arg Ala Ala Leu Thr Arg Ile Ile Thr Ser Tyr Ala Glu Ser Ser Gly 195 200 205 atc ctg aag aag gaa aag gtc agc ctg ggc ggc gaa gac agc cgc gag 672 Ile Leu Lys Lys Glu Lys Val Ser Leu Gly Gly Glu Asp Ser Arg Glu 210 215 220 ggc ctg acc tgc gtg ctg tcg gtc 696 Gly Leu Thr Cys Val Leu Ser Val 225 230 16 232 PRT Caulobacter crescentus 16 Gln Asn Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val Ser 1 5 10 15 Val Val Asn Ala Leu Ser Asp Trp Leu Glu Leu Leu Ile His Arg Asn 20 25 30 Gly Lys Val His Gln Met Arg Phe Glu Arg Gly Asp Ala Val Thr Ser 35 40 45 Leu Lys Val Thr Gly Asp Ser Pro Val Arg Thr Glu Gly Pro Lys Ala 50 55 60 Gly Glu Thr Leu Thr Gly Thr Glu Val Thr Phe Phe Pro Ser Lys Asp 65 70 75 80 Thr Phe Ala Phe Ile Glu Phe Asp Arg Lys Thr Leu Glu His Arg Leu 85 90 95 Arg Glu Leu Ala Phe Leu Asn Ser Gly Val Thr Ile Trp Phe Lys Asp 100 105 110 His Arg Asp Val Glu Pro Trp Glu Glu Lys Leu Phe Tyr Glu Gly Gly 115 120 125 Ile Glu Ala Phe Val Arg His Leu Asp Lys Ala Lys Thr Pro Leu Leu 130 135 140 Lys Ala Pro Ile Ala Val Lys Gly Val Lys Asp Lys Val Glu Ile Asp 145 150 155 160 Leu Ala Leu Trp Trp Asn Asp Ser Tyr His Glu Gln Met Leu Cys Phe 165 170 175 Thr Asn Asn Ile Pro Gln Arg Asp Gly Gly Thr His Leu Ser Ala Phe 180 185 190 Arg Ala Ala Leu Thr Arg Ile Ile Thr Ser Tyr Ala Glu Ser Ser Gly 195 200 205 Ile Leu Lys Lys Glu Lys Val Ser Leu Gly Gly Glu Asp Ser Arg Glu 210 215 220 Gly Leu Thr Cys Val Leu Ser Val 225 230 17 888 DNA Pseudomonas putida CDS (1)...(888) 17 ggc ggc ctg cac ggt gta ggc gtg tcg gta gtg aac gca ctg tct gaa 48 Gly Gly Leu His Gly Val Gly Val Ser Val Val Asn Ala Leu Ser Glu 1 5 10 15 gag ctc gtc ctc acc gtt cgc cgt agc ggc aag atc tgg gaa cag acc 96 Glu Leu Val Leu Thr Val Arg Arg Ser Gly Lys Ile Trp Glu Gln Thr 20 25 30 tac gtc cat ggt gtt ccg cag gaa ccg atg aag atc gtt ggc gac agc 144 Tyr Val His Gly Val Pro Gln Glu Pro Met Lys Ile Val Gly Asp Ser 35 40 45 gaa acc acc ggc acc cag atc cac ttc aag gct tcc agc gaa acc ttc 192 Glu Thr Thr Gly Thr Gln Ile His Phe Lys Ala Ser Ser Glu Thr Phe 50 55 60 aag aac atc cac ttc agc tgg gac atc ctg gcc aag cgg att cgt gaa 240 Lys Asn Ile His Phe Ser Trp Asp Ile Leu Ala Lys Arg Ile Arg Glu 65 70 75 80 ctg tcc ttc ctc aac tcc ggt gtc ggc atc gtc ctc aag gat gag cgc 288 Leu Ser Phe Leu Asn Ser Gly Val Gly Ile Val Leu Lys Asp Glu Arg 85 90 95 agc ggc aag gaa gaa ctg ttc aag tac gaa ggc ggc ttg cgc gcg ttc 336 Ser Gly Lys Glu Glu Leu Phe Lys Tyr Glu Gly Gly Leu Arg Ala Phe 100 105 110 gtt gaa tac ctg aac acc aac aag acc ccg gtc aac cag gtg ttc cat 384 Val Glu Tyr Leu Asn Thr Asn Lys Thr Pro Val Asn Gln Val Phe His 115 120 125 ttc aac atc cag cgc gaa gac ggc atc ggc gta gaa atc gcc ctg cag 432 Phe Asn Ile Gln Arg Glu Asp Gly Ile Gly Val Glu Ile Ala Leu Gln 130 135 140 tgg aac gac agc ttc aac gag aac ctg ttg tgc ttc acc aac aac att 480 Trp Asn Asp Ser Phe Asn Glu Asn Leu Leu Cys Phe Thr Asn Asn Ile 145 150 155 160 ccg cag cgc gat ggc ggt act cac ctg gtg ggt ttc cgt tcc gcc ctg 528 Pro Gln Arg Asp Gly Gly Thr His Leu Val Gly Phe Arg Ser Ala Leu 165 170 175 acg cgt aac ctc aat acg tat atc gaa gcc gaa ggc ctg gcg aag aag 576 Thr Arg Asn Leu Asn Thr Tyr Ile Glu Ala Glu Gly Leu Ala Lys Lys 180 185 190 cac aag gtc gcg acc acc ggt gac gat gcc cgt gaa ggc ctg gcc gcg 624 His Lys Val Ala Thr Thr Gly Asp Asp Ala Arg Glu Gly Leu Ala Ala 195 200 205 atc att tcg gta aaa gtg ccg gat ccg aag ttc agc tcc cag acc aag 672 Ile Ile Ser Val Lys Val Pro Asp Pro Lys Phe Ser Ser Gln Thr Lys 210 215 220 gac aag ctg gtt tct tcc gaa gtg aag acc gcg gtc gaa cag gaa atg 720 Asp Lys Leu Val Ser Ser Glu Val Lys Thr Ala Val Glu Gln Glu Met 225 230 235 240 ggc aag tac ttc tcc gac ttc ctg ctg gaa aac ccg aac gaa gcc aag 768 Gly Lys Tyr Phe Ser Asp Phe Leu Leu Glu Asn Pro Asn Glu Ala Lys 245 250 255 ctg gtt gtc ggc aag atg atc gac gcg gca cgt gct cgt gaa gcg gcg 816 Leu Val Val Gly Lys Met Ile Asp Ala Ala Arg Ala Arg Glu Ala Ala 260 265 270 cgc aag acc cgt gag atg acc cgc cgc aaa ggc gcg ctg gac atc gcc 864 Arg Lys Thr Arg Glu Met Thr Arg Arg Lys Gly Ala Leu Asp Ile Ala 275 280 285 ggc ctg ccg ggc aaa ctg gct gac 888 Gly Leu Pro Gly Lys Leu Ala Asp 290 295 18 296 PRT Pseudomonas putida 18 Gly Gly Leu His Gly Val Gly Val Ser Val Val Asn Ala Leu Ser Glu 1 5 10 15 Glu Leu Val Leu Thr Val Arg Arg Ser Gly Lys Ile Trp Glu Gln Thr 20 25 30 Tyr Val His Gly Val Pro Gln Glu Pro Met Lys Ile Val Gly Asp Ser 35 40 45 Glu Thr Thr Gly Thr Gln Ile His Phe Lys Ala Ser Ser Glu Thr Phe 50 55 60 Lys Asn Ile His Phe Ser Trp Asp Ile Leu Ala Lys Arg Ile Arg Glu 65 70 75 80 Leu Ser Phe Leu Asn Ser Gly Val Gly Ile Val Leu Lys Asp Glu Arg 85 90 95 Ser Gly Lys Glu Glu Leu Phe Lys Tyr Glu Gly Gly Leu Arg Ala Phe 100 105 110 Val Glu Tyr Leu Asn Thr Asn Lys Thr Pro Val Asn Gln Val Phe His 115 120 125 Phe Asn Ile Gln Arg Glu Asp Gly Ile Gly Val Glu Ile Ala Leu Gln 130 135 140 Trp Asn Asp Ser Phe Asn Glu Asn Leu Leu Cys Phe Thr Asn Asn Ile 145 150 155 160 Pro Gln Arg Asp Gly Gly Thr His Leu Val Gly Phe Arg Ser Ala Leu 165 170 175 Thr Arg Asn Leu Asn Thr Tyr Ile Glu Ala Glu Gly Leu Ala Lys Lys 180 185 190 His Lys Val Ala Thr Thr Gly Asp Asp Ala Arg Glu Gly Leu Ala Ala 195 200 205 Ile Ile Ser Val Lys Val Pro Asp Pro Lys Phe Ser Ser Gln Thr Lys 210 215 220 Asp Lys Leu Val Ser Ser Glu Val Lys Thr Ala Val Glu Gln Glu Met 225 230 235 240 Gly Lys Tyr Phe Ser Asp Phe Leu Leu Glu Asn Pro Asn Glu Ala Lys 245 250 255 Leu Val Val Gly Lys Met Ile Asp Ala Ala Arg Ala Arg Glu Ala Ala 260 265 270 Arg Lys Thr Arg Glu Met Thr Arg Arg Lys Gly Ala Leu Asp Ile Ala 275 280 285 Gly Leu Pro Gly Lys Leu Ala Asp 290 295 19 531 DNA Synechococcus sp. CDS (1)...(531) 19 ttg gtg cgt cgc aaa tca gtg ctg gaa tct tcg aca ttg ccc ggt aaa 48 Leu Val Arg Arg Lys Ser Val Leu Glu Ser Ser Thr Leu Pro Gly Lys 1 5 10 15 tta gca gac tgt tcc agt cgc gat ccc ggt gaa tct gaa atc ttc atc 96 Leu Ala Asp Cys Ser Ser Arg Asp Pro Gly Glu Ser Glu Ile Phe Ile 20 25 30 gtg gaa ggg gat tcg gca ggt ggc agt gct aaa cag ggg cgc gat cgc 144 Val Glu Gly Asp Ser Ala Gly Gly Ser Ala Lys Gln Gly Arg Asp Arg 35 40 45 cgc ttc caa gcc atc ctg cct ctg cgc ggc aaa atc ctc aac atc gag 192 Arg Phe Gln Ala Ile Leu Pro Leu Arg Gly Lys Ile Leu Asn Ile Glu 50 55 60 aaa acg gac gat gcc aaa atc tac aaa aac act gag atc caa gcc ctg 240 Lys Thr Asp Asp Ala Lys Ile Tyr Lys Asn Thr Glu Ile Gln Ala Leu 65 70 75 80 att aca gcg ctg ggc ctc gga att aaa ggg gag gaa ttt gat gct tcc 288 Ile Thr Ala Leu Gly Leu Gly Ile Lys Gly Glu Glu Phe Asp Ala Ser 85 90 95 caa ctg cgc tac cac cgt att gtg atc atg act gac gcg gac gtc gat 336 Gln Leu Arg Tyr His Arg Ile Val Ile Met Thr Asp Ala Asp Val Asp 100 105 110 ggt gcg cac atc cgt acc ctc ttg ctc acc ttc ttc tat cgc tat cag 384 Gly Ala His Ile Arg Thr Leu Leu Leu Thr Phe Phe Tyr Arg Tyr Gln 115 120 125 cga tcg ctg ctg gag cag ggc tac atg tac att gcc tgc ccg ccg ctg 432 Arg Ser Leu Leu Glu Gln Gly Tyr Met Tyr Ile Ala Cys Pro Pro Leu 130 135 140 tac aag ttg gag cgg gga cgt aat cac tac tat tgc tac aac gaa cgc 480 Tyr Lys Leu Glu Arg Gly Arg Asn His Tyr Tyr Cys Tyr Asn Glu Arg 145 150 155 160 gaa ctg cag gaa cgg att gcg acg ttc cct gaa aac gcc aac tat acg 528 Glu Leu Gln Glu Arg Ile Ala Thr Phe Pro Glu Asn Ala Asn Tyr Thr 165 170 175 att 531 Ile 20 177 PRT Synechococcus sp. 20 Leu Val Arg Arg Lys Ser Val Leu Glu Ser Ser Thr Leu Pro Gly Lys 1 5 10 15 Leu Ala Asp Cys Ser Ser Arg Asp Pro Gly Glu Ser Glu Ile Phe Ile 20 25 30 Val Glu Gly Asp Ser Ala Gly Gly Ser Ala Lys Gln Gly Arg Asp Arg 35 40 45 Arg Phe Gln Ala Ile Leu Pro Leu Arg Gly Lys Ile Leu Asn Ile Glu 50 55 60 Lys Thr Asp Asp Ala Lys Ile Tyr Lys Asn Thr Glu Ile Gln Ala Leu 65 70 75 80 Ile Thr Ala Leu Gly Leu Gly Ile Lys Gly Glu Glu Phe Asp Ala Ser 85 90 95 Gln Leu Arg Tyr His Arg Ile Val Ile Met Thr Asp Ala Asp Val Asp 100 105 110 Gly Ala His Ile Arg Thr Leu Leu Leu Thr Phe Phe Tyr Arg Tyr Gln 115 120 125 Arg Ser Leu Leu Glu Gln Gly Tyr Met Tyr Ile Ala Cys Pro Pro Leu 130 135 140 Tyr Lys Leu Glu Arg Gly Arg Asn His Tyr Tyr Cys Tyr Asn Glu Arg 145 150 155 160 Glu Leu Gln Glu Arg Ile Ala Thr Phe Pro Glu Asn Ala Asn Tyr Thr 165 170 175 Ile 21 660 DNA Caulobacter crescentus CDS (1)...(660) 21 cgg gat ggc ggc acg cac ctg tcg gcc ttt cgc gcg gcc ctg acc cgg 48 Arg Asp Gly Gly Thr His Leu Ser Ala Phe Arg Ala Ala Leu Thr Arg 1 5 10 15 atc atc acc agc tac gcc gag agc tcc ggc atc ctg aag aag gaa aag 96 Ile Ile Thr Ser Tyr Ala Glu Ser Ser Gly Ile Leu Lys Lys Glu Lys 20 25 30 gtc agc ctg ggc ggc gaa gac agc cgc gag ggc ctg acc tgc gtg ctg 144 Val Ser Leu Gly Gly Glu Asp Ser Arg Glu Gly Leu Thr Cys Val Leu 35 40 45 tcg gtc aag gtc ccg gat ccg aag ttc agc tcg cag acc aag gac aag 192 Ser Val Lys Val Pro Asp Pro Lys Phe Ser Ser Gln Thr Lys Asp Lys 50 55 60 ctg gtc tcg tcc gaa gtg cgc ccc gcc gtt gag ggc ctg gtg tcg gaa 240 Leu Val Ser Ser Glu Val Arg Pro Ala Val Glu Gly Leu Val Ser Glu 65 70 75 80 ggt ctc tcg acc tgg ttc gag gaa cat ccg aac gag gcc aag gcg atc 288 Gly Leu Ser Thr Trp Phe Glu Glu His Pro Asn Glu Ala Lys Ala Ile 85 90 95 gtg acc aag atc gcc gag gcc gcc gcc gcc cgc gag gcc gcc cgc aag 336 Val Thr Lys Ile Ala Glu Ala Ala Ala Ala Arg Glu Ala Ala Arg Lys 100 105 110 gcg cga gag ctg acc cgc cgc aag agc gcg ctc gac atc acc agc ctg 384 Ala Arg Glu Leu Thr Arg Arg Lys Ser Ala Leu Asp Ile Thr Ser Leu 115 120 125 ccc ggc aag ctc gcc gac tgc tcg gaa cgc gat ccg gcc aag tcc gag 432 Pro Gly Lys Leu Ala Asp Cys Ser Glu Arg Asp Pro Ala Lys Ser Glu 130 135 140 atc ttc atc gtc gag ggc gac tcg gcg ggc ggc tcg gcc aag cag gcc 480 Ile Phe Ile Val Glu Gly Asp Ser Ala Gly Gly Ser Ala Lys Gln Ala 145 150 155 160 cgc aac cgc gac aac cag gcc gtt ctg ccc ctg cgc ggc aag atc ctg 528 Arg Asn Arg Asp Asn Gln Ala Val Leu Pro Leu Arg Gly Lys Ile Leu 165 170 175 aac gtc gag cgg gcc cgc ttc gac aag atg ctg tcg tcc gac cag atc 576 Asn Val Glu Arg Ala Arg Phe Asp Lys Met Leu Ser Ser Asp Gln Ile 180 185 190 ggc acg ctg atc acc gcc ctg ggc gcg ggg atc ggc cgc gac gac ttc 624 Gly Thr Leu Ile Thr Ala Leu Gly Ala Gly Ile Gly Arg Asp Asp Phe 195 200 205 aac ccg gac aag gtg cgc tac cac aag atc gtg ctg 660 Asn Pro Asp Lys Val Arg Tyr His Lys Ile Val Leu 210 215 220 22 220 PRT Caulobacter crescentus 22 Arg Asp Gly Gly Thr His Leu Ser Ala Phe Arg Ala Ala Leu Thr Arg 1 5 10 15 Ile Ile Thr Ser Tyr Ala Glu Ser Ser Gly Ile Leu Lys Lys Glu Lys 20 25 30 Val Ser Leu Gly Gly Glu Asp Ser Arg Glu Gly Leu Thr Cys Val Leu 35 40 45 Ser Val Lys Val Pro Asp Pro Lys Phe Ser Ser Gln Thr Lys Asp Lys 50 55 60 Leu Val Ser Ser Glu Val Arg Pro Ala Val Glu Gly Leu Val Ser Glu 65 70 75 80 Gly Leu Ser Thr Trp Phe Glu Glu His Pro Asn Glu Ala Lys Ala Ile 85 90 95 Val Thr Lys Ile Ala Glu Ala Ala Ala Ala Arg Glu Ala Ala Arg Lys 100 105 110 Ala Arg Glu Leu Thr Arg Arg Lys Ser Ala Leu Asp Ile Thr Ser Leu 115 120 125 Pro Gly Lys Leu Ala Asp Cys Ser Glu Arg Asp Pro Ala Lys Ser Glu 130 135 140 Ile Phe Ile Val Glu Gly Asp Ser Ala Gly Gly Ser Ala Lys Gln Ala 145 150 155 160 Arg Asn Arg Asp Asn Gln Ala Val Leu Pro Leu Arg Gly Lys Ile Leu 165 170 175 Asn Val Glu Arg Ala Arg Phe Asp Lys Met Leu Ser Ser Asp Gln Ile 180 185 190 Gly Thr Leu Ile Thr Ala Leu Gly Ala Gly Ile Gly Arg Asp Asp Phe 195 200 205 Asn Pro Asp Lys Val Arg Tyr His Lys Ile Val Leu 210 215 220 23 1422 DNA Cytophaga lytica CDS (1)...(1422) 23 gat aaa gat tca tac aaa gta tct ggt ggt tta cac ggt gta ggt gta 48 Asp Lys Asp Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val 1 5 10 15 tct tgt gta aac gca tta tct aat aat tta aaa gct act gtt tac aga 96 Ser Cys Val Asn Ala Leu Ser Asn Asn Leu Lys Ala Thr Val Tyr Arg 20 25 30 gaa ggt aaa ata tgg gag caa gag tat gaa aga ggt aag gct tta tat 144 Glu Gly Lys Ile Trp Glu Gln Glu Tyr Glu Arg Gly Lys Ala Leu Tyr 35 40 45 ccg gta aaa agt att gga gaa aca gag gaa aca ggt act ata gtt act 192 Pro Val Lys Ser Ile Gly Glu Thr Glu Glu Thr Gly Thr Ile Val Thr 50 55 60 ttt tac cca gat gat act ata ttt aca caa act aca gag tat aat tat 240 Phe Tyr Pro Asp Asp Thr Ile Phe Thr Gln Thr Thr Glu Tyr Asn Tyr 65 70 75 80 gaa acg ctt tct aac aga atg cga gag ttg gct tac ctt aat aag gga 288 Glu Thr Leu Ser Asn Arg Met Arg Glu Leu Ala Tyr Leu Asn Lys Gly 85 90 95 gtt aca att agc att aca gat aag aga gtt aaa gat gaa aag gga gag 336 Val Thr Ile Ser Ile Thr Asp Lys Arg Val Lys Asp Glu Lys Gly Glu 100 105 110 ttt tta tct gaa gtt ttt tac tct gaa gaa gga cta aaa gaa ttt att 384 Phe Leu Ser Glu Val Phe Tyr Ser Glu Glu Gly Leu Lys Glu Phe Ile 115 120 125 aag ttt tta gac ggt aac aga gaa caa cta ata cgt gat gtt gtt tca 432 Lys Phe Leu Asp Gly Asn Arg Glu Gln Leu Ile Arg Asp Val Val Ser 130 135 140 atg gaa ggt gaa aaa aac gga att cct gtt gag gtt gca atg gtg tac 480 Met Glu Gly Glu Lys Asn Gly Ile Pro Val Glu Val Ala Met Val Tyr 145 150 155 160 aat aca tca tat tca gaa aat ctt cac tct tac gta aat aat att aat 528 Asn Thr Ser Tyr Ser Glu Asn Leu His Ser Tyr Val Asn Asn Ile Asn 165 170 175 aca cat gaa ggt ggt aca cac ctt tca ggt ttt aga aga ggt tta aca 576 Thr His Glu Gly Gly Thr His Leu Ser Gly Phe Arg Arg Gly Leu Thr 180 185 190 tca acc tta aaa aag tat gca gat gca tct gga atg tta gac aaa tta 624 Ser Thr Leu Lys Lys Tyr Ala Asp Ala Ser Gly Met Leu Asp Lys Leu 195 200 205 aag ttt gag att cag gga gat gat ttt aga gaa ggt tta acg gct att 672 Lys Phe Glu Ile Gln Gly Asp Asp Phe Arg Glu Gly Leu Thr Ala Ile 210 215 220 gtg tct gtt aaa gtt gca gaa cct cag ttt gaa ggg caa aca aaa act 720 Val Ser Val Lys Val Ala Glu Pro Gln Phe Glu Gly Gln Thr Lys Thr 225 230 235 240 aaa tta ggt aac aga gaa gtt tct tct gca gtg agc caa gct gta tca 768 Lys Leu Gly Asn Arg Glu Val Ser Ser Ala Val Ser Gln Ala Val Ser 245 250 255 gaa atg ctt acc aac tat tta gaa gaa aac cca gat gat gct aag gta 816 Glu Met Leu Thr Asn Tyr Leu Glu Glu Asn Pro Asp Asp Ala Lys Val 260 265 270 att gta caa aaa gtc att ttg gca gcg caa gca cgt cat gcg gct aca 864 Ile Val Gln Lys Val Ile Leu Ala Ala Gln Ala Arg His Ala Ala Thr 275 280 285 aaa gcc cgt gaa atg gta cag cgt aaa acg gta atg agt ata ggt ggt 912 Lys Ala Arg Glu Met Val Gln Arg Lys Thr Val Met Ser Ile Gly Gly 290 295 300 tta cca ggg aaa tta tca gac tgt tct gag caa gat gct aca aaa tgc 960 Leu Pro Gly Lys Leu Ser Asp Cys Ser Glu Gln Asp Ala Thr Lys Cys 305 310 315 320 gaa gta ttc ctt gta gag gga gat tcg gcg ggt ggt act gct aaa caa 1008 Glu Val Phe Leu Val Glu Gly Asp Ser Ala Gly Gly Thr Ala Lys Gln 325 330 335 ggt agg gac aga aac ttt cag gca ata tta ccg ctt cgt ggt aaa atc 1056 Gly Arg Asp Arg Asn Phe Gln Ala Ile Leu Pro Leu Arg Gly Lys Ile 340 345 350 tta aat gtt gaa aaa gca atg caa cat aag gtt ttt gaa aac gaa gaa 1104 Leu Asn Val Glu Lys Ala Met Gln His Lys Val Phe Glu Asn Glu Glu 355 360 365 ata aaa aat att tac aca gct tta ggt gtt act att ggt aca gaa gaa 1152 Ile Lys Asn Ile Tyr Thr Ala Leu Gly Val Thr Ile Gly Thr Glu Glu 370 375 380 gat agt aaa gcc tta aac tta gaa aaa tta aga tac cat aaa gta gtt 1200 Asp Ser Lys Ala Leu Asn Leu Glu Lys Leu Arg Tyr His Lys Val Val 385 390 395 400 att atg tgt gat gcc gat gta gat ggt agc cac att gaa act tta atc 1248 Ile Met Cys Asp Ala Asp Val Asp Gly Ser His Ile Glu Thr Leu Ile 405 410 415 ctt aca ttc ttc ttc cgt ttt atg agg gag tta ata gaa ggc ggt cac 1296 Leu Thr Phe Phe Phe Arg Phe Met Arg Glu Leu Ile Glu Gly Gly His 420 425 430 gtt tat ata gca acc cca cct tta tac ttg gta aaa aag gga aca aaa 1344 Val Tyr Ile Ala Thr Pro Pro Leu Tyr Leu Val Lys Lys Gly Thr Lys 435 440 445 aaa cgt tat gct tgg aat gat aaa gaa cga gat gag ata gca gaa agc 1392 Lys Arg Tyr Ala Trp Asn Asp Lys Glu Arg Asp Glu Ile Ala Glu Ser 450 455 460 ttt aat ggt agt gtt ggt ata caa aga tat 1422 Phe Asn Gly Ser Val Gly Ile Gln Arg Tyr 465 470 24 474 PRT Cytophaga lytica 24 Asp Lys Asp Ser Tyr Lys Val Ser Gly Gly Leu His Gly Val Gly Val 1 5 10 15 Ser Cys Val Asn Ala Leu Ser Asn Asn Leu Lys Ala Thr Val Tyr Arg 20 25 30 Glu Gly Lys Ile Trp Glu Gln Glu Tyr Glu Arg Gly Lys Ala Leu Tyr 35 40 45 Pro Val Lys Ser Ile Gly Glu Thr Glu Glu Thr Gly Thr Ile Val Thr 50 55 60 Phe Tyr Pro Asp Asp Thr Ile Phe Thr Gln Thr Thr Glu Tyr Asn Tyr 65 70 75 80 Glu Thr Leu Ser Asn Arg Met Arg Glu Leu Ala Tyr Leu Asn Lys Gly 85 90 95 Val Thr Ile Ser Ile Thr Asp Lys Arg Val Lys Asp Glu Lys Gly Glu 100 105 110 Phe Leu Ser Glu Val Phe Tyr Ser Glu Glu Gly Leu Lys Glu Phe Ile 115 120 125 Lys Phe Leu Asp Gly Asn Arg Glu Gln Leu Ile Arg Asp Val Val Ser 130 135 140 Met Glu Gly Glu Lys Asn Gly Ile Pro Val Glu Val Ala Met Val Tyr 145 150 155 160 Asn Thr Ser Tyr Ser Glu Asn Leu His Ser Tyr Val Asn Asn Ile Asn 165 170 175 Thr His Glu Gly Gly Thr His Leu Ser Gly Phe Arg Arg Gly Leu Thr 180 185 190 Ser Thr Leu Lys Lys Tyr Ala Asp Ala Ser Gly Met Leu Asp Lys Leu 195 200 205 Lys Phe Glu Ile Gln Gly Asp Asp Phe Arg Glu Gly Leu Thr Ala Ile 210 215 220 Val Ser Val Lys Val Ala Glu Pro Gln Phe Glu Gly Gln Thr Lys Thr 225 230 235 240 Lys Leu Gly Asn Arg Glu Val Ser Ser Ala Val Ser Gln Ala Val Ser 245 250 255 Glu Met Leu Thr Asn Tyr Leu Glu Glu Asn Pro Asp Asp Ala Lys Val 260 265 270 Ile Val Gln Lys Val Ile Leu Ala Ala Gln Ala Arg His Ala Ala Thr 275 280 285 Lys Ala Arg Glu Met Val Gln Arg Lys Thr Val Met Ser Ile Gly Gly 290 295 300 Leu Pro Gly Lys Leu Ser Asp Cys Ser Glu Gln Asp Ala Thr Lys Cys 305 310 315 320 Glu Val Phe Leu Val Glu Gly Asp Ser Ala Gly Gly Thr Ala Lys Gln 325 330 335 Gly Arg Asp Arg Asn Phe Gln Ala Ile Leu Pro Leu Arg Gly Lys Ile 340 345 350 Leu Asn Val Glu Lys Ala Met Gln His Lys Val Phe Glu Asn Glu Glu 355 360 365 Ile Lys Asn Ile Tyr Thr Ala Leu Gly Val Thr Ile Gly Thr Glu Glu 370 375 380 Asp Ser Lys Ala Leu Asn Leu Glu Lys Leu Arg Tyr His Lys Val Val 385 390 395 400 Ile Met Cys Asp Ala Asp Val Asp Gly Ser His Ile Glu Thr Leu Ile 405 410 415 Leu Thr Phe Phe Phe Arg Phe Met Arg Glu Leu Ile Glu Gly Gly His 420 425 430 Val Tyr Ile Ala Thr Pro Pro Leu Tyr Leu Val Lys Lys Gly Thr Lys 435 440 445 Lys Arg Tyr Ala Trp Asn Asp Lys Glu Arg Asp Glu Ile Ala Glu Ser 450 455 460 Phe Asn Gly Ser Val Gly Ile Gln Arg Tyr 465 470 25 38 DNA Artificial Sequence oligonucleotide for PCR 25 tgtaaaacga cggccagtca ygcnggnggn aarttyga 38 26 7 PRT Artificial Sequence synthetically generated peptide 26 His Ala Gly Gly Lys Phe Asp 1 5 27 36 DNA Artificial Sequence oligonucleotide for PCR 27 ctgcgttcgt atatgagcnc crtcnacrtc ngcrtc 36 28 12 PRT Artificial Sequence synthetically generated peptide 28 Asp Ala Asp Val Asp Gly Ala His Ile Arg Thr Leu 1 5 10 29 41 DNA Artificial Sequence oligonucleotide for PCR 29 gaagtcatca tgaccgttct gcaygsnggn ggnaarttyg g 41 30 14 PRT Artificial Sequence synthetically generated peptide 30 Glu Val Leu Met Thr Val Leu His Ala Gly Gly Lys Phe Gly 1 5 10 31 44 DNA Artificial Sequence oligonucleotide for PCR 31 agcagggtac ggatgtgcga gccrtcnacr tcngcrtcng tgat 44 32 15 PRT Artificial Sequence synthetically generated peptide 32 Met Thr Asp Ala Asp Val Asp Gly Ser His Ile Arg Thr Leu Leu 1 5 10 15 33 32 DNA Artificial Sequence oligonucleotide for PCR 33 caggaaacag ctatgaccar rtgngtnccn cc 32 34 5 PRT Artificial Sequence synthetically generated peptide 34 Gly Gly Thr His Leu 1 5 35 34 DNA Artificial Sequence oligonucleotide for PCR 35 gcaacgagat caacactcmn garggnggna cnca 34 36 11 PRT Artificial Sequence synthetically generated peptide 36 Asn Asn Ile Asn Thr His Glu Gly Gly Thr His 1 5 10 37 11 PRT Artificial Sequence synthetically generated peptide 37 Asn Asn Ile Asn Thr Pro Glu Gly Gly Thr His 1 5 10 38 35 DNA Artificial Sequence oligonucleotide for PCR 38 tgtaaaacga cggccagtar yttnkyyttn gtytg 35 39 6 PRT Artificial Sequence synthetically generated peptide 39 Gln Thr Lys Thr Lys Leu 1 5 40 6 PRT Artificial Sequence synthetically generated peptide 40 Gln Thr Lys Asp Lys Leu 1 5 41 35 DNA Artificial Sequence oligonucleotide for PCR 41 taggctagct gaccgtaaga ygcngayrtn gaygg 35 42 6 PRT Artificial Sequence synthetically generated peptide 42 Asp Ala Asp Val Asp Gly 1 5 43 36 DNA Artificial Sequence oligonucleotide for PCR 43 ccatagctgc gtagcattca tytcnccnar nccytt 36 44 12 PRT Artificial Sequence synthetically generated peptide 44 Lys Gly Leu Gly Glu Met Asn Ala Thr Gln Leu Trp 1 5 10 45 41 DNA Artificial Sequence oligonucleotide for PCR 45 caggaaacag ctatgaccaa rmgnccngsn atgtayathg g 41 46 8 PRT Artificial Sequence synthetically generated peptide 46 Lys Arg Pro Ala Met Tyr Ile Gly 1 5 47 8 PRT Artificial Sequence synthetically generated peptide 47 Lys Arg Pro Gly Met Tyr Ile Gly 1 5 48 38 DNA Artificial Sequence oligonucleotide for PCR 48 tgtaaaacga cggccagtcc nccngcnswr tcnccytc 38 49 7 PRT Artificial Sequence synthetically generated peptide 49 Glu Gly Asp Ser Ala Gly Gly 1 5 50 39 DNA Artificial Sequence oligonucleotide for PCR 50 tgtaaaacga cggccagtca tngtngtntc ccanarytg 39 51 7 PRT Artificial Sequence synthetically generated peptide 51 Gln Leu Trp Glu Thr Thr Met 1 5 52 7 PRT Artificial Sequence synthetically generated peptide 52 Gln Leu Trp Asp Thr Thr Met 1 5 53 41 DNA Artificial Sequence oligonucleotide for PCR 53 gaagtcatca tgaccgttct gcaygcnggn ggnaarttyg a 41 54 14 PRT Artificial Sequence synthetically generated peptide 54 Glu Val Ile Met Thr Val Leu His Ala Gly Gly Lys Phe Asp 1 5 10 55 14 PRT Artificial Sequence synthetically generated peptide 55 Glu Val Ile Met Thr Val Leu His Ala Gly Gly Lys Phe Asn 1 5 10 56 14 PRT Artificial Sequence synthetically generated peptide 56 Glu Val Ile Met Thr Val Leu His Ala Gly Gly Lys Phe Glu 1 5 10 57 14 PRT Artificial Sequence synthetically generated peptide 57 Glu Val Ile Met Thr Val Leu His Ala Gly Gly Lys Phe Lys 1 5 10 58 38 DNA Artificial Sequence oligonucleotide for PCR 58 tgtaaaacga cggccagtgc nggrtcytty tcytgrca 38 59 7 PRT Artificial Sequence synthetically generated peptide 59 Cys Gln Glu Lys Asp Pro Ala 1 5 60 40 DNA Artificial Sequence oligonucleotide for PCR 60 gaagtcatca tgaccgttct gcaacnaaya ayathccnca 40 61 6 PRT Artificial Sequence synthetically generated peptide 61 Thr Asn Asn Ile Pro Gln 1 5 62 38 DNA Artificial Sequence oligonucleotide for PCR 62 tgtaaaacga cggccagtaa yttnggntcn ggnacytt 38 63 7 PRT Artificial Sequence synthetically generated peptide 63 Lys Val Pro Asp Pro Lys Phe 1 5 64 7 PRT Artificial Sequence synthetically generated peptide 64 Lys Val Pro Glu Pro Lys Phe 1 5 65 35 DNA Artificial Sequence oligonucleotide for PCR 65 caggaaacag ctatgaccgc nmrnmrngcn mgnga 35 66 6 PRT Artificial Sequence synthetically generated peptide 66 Ala Arg Arg Ala Arg Glu 1 5 67 6 PRT Artificial Sequence synthetically generated peptide 67 Ala Arg Lys Ala Arg Glu 1 5 68 6 PRT Artificial Sequence synthetically generated peptide 68 Ala Lys Lys Ala Arg Glu 1 5 69 19 PRT Artificial Sequence synthetically generated peptide 69 Xaa Xaa Xaa Xaa Xaa Xaa Xaa Thr Xaa Leu His Ala Gly Gly Lys Phe 1 5 10 15 Xaa Xaa Xaa 70 4 PRT Artificial Sequence synthetically generated peptide 70 Gly Gly Thr His 1 71 15 PRT Artificial Sequence synthetically generated peptide 71 Xaa Met Thr Asp Ala Asp Val Asp Gly Xaa His Ile Arg Thr Leu 1 5 10 15 72 11 PRT Artificial Sequence synthetically generated peptide 72 Arg Lys Arg Pro Xaa Met Tyr Ile Gly Xaa Thr 1 5 10 73 6 PRT Artificial Sequence synthetically generated peptide 73 Gln Xaa Xaa Xaa Lys Leu 1 5 74 9 PRT Artificial Sequence synthetically generated peptide 74 Xaa Lys Gly Leu Gly Glu Met Asn Xaa 1 5 75 9 PRT Artificial Sequence synthetically generated peptide 75 Val Glu Gly Asp Ser Ala Gly Gly Ser 1 5 76 7 PRT Artificial Sequence synthetically generated peptide 76 Lys Xaa Pro Asp Pro Xaa Phe 1 5 77 14 PRT Artificial Sequence synthetically generated peptide 77 Leu Pro Gly Lys Leu Ala Asp Cys Xaa Xaa Xaa Asp Pro Xaa 1 5 10 78 9 PRT Artificial Sequence synthetically generated peptide 78 Gln Leu Xaa Xaa Thr Thr Xaa Xaa Pro 1 5 79 6 PRT Artificial Sequence synthetically generated peptide 79 Ala Xaa Xaa Ala Arg Glu 1 5 80 7 PRT Artificial Sequence synthetically generated peptide 80 Phe Thr Asn Asn Ile Xaa Xaa 1 5 81 7 PRT Pseudomonas putida 81 His Ala Gly Gly Lys Phe Asp 1 5 82 8 PRT Pseudomonas putida 82 Met Thr Asp Ala Asp Val Asp Gly 1 5 

What is claimed is:
 1. A method for identifying a microorganism, comprising the following steps (1) to (5): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of the sequence pairs (69) and (74), (69) and (78), (72) and (71), (72) and (74), and (72) and (78); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) isolating said DNA fragment; (4) determining the nucleotide sequence of said DNA fragment; and (5) identifying the microorganism by comparing the sequence of the amplified gyrB gene DNA fragment to known gyrB gene DNA fragment sequences.
 2. The method for identifying a microorganism according to claim 1, wherein the amino acid sequence pairs that are used are sequence pairs (69) and (74), (69) and (78), (72) and (74), or (72) and (78); and said microorganism belongs to proteobacteria.
 3. A method for identifying a microorganism, comprising the following steps (1) to (8): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (71); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (73); (4) synthesizing forward and reverse primers based on a single pair of amino acid sequences (70) and (71); (5) amplifying the gyrB gene DNA fragment produced in step (2) using said two pairs of primers, so that two gyrB gene DNA fragments are produced; (6) isolating said two DNA fragments; (7) determining the nucleotide sequences of said two DNA fragments; and (8) identifying the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 4. A method for identifying a microorganism, comprising the following steps (1) to (8): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (74); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (73); (4) synthesizing forward and reverse primers based on a single pair of amino acid sequences (70) and (74); (5) amplifying the gyrB gene DNA fragment produced in step (2) using said two pairs of primers, so that two gyrB gene DNA fragments are produced; (6) isolating said two DNA fragments; (7) determining the nucleotide sequences of said two DNA fragments; and (8) identifying the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 5. A method for identifying a microorganism, comprising the following steps (1) to (8): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (72) and (74); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) synthesizing forward and reverse primers based on a single pair of amino acid sequences (72) and (73); (4) synthesizing forward and reverse primers based on a single pair of amino acid sequences (70) and (74); (5) amplifying the gyrB gene DNA fragment produced in step (2) using said two pairs of primers, so that two gyrB gene DNA fragments are produced; (6) isolating said two DNA fragments; (7) determining the nucleotide sequences of said two DNA fragments; and (8) identifying the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 6. A method for identifying a microorganism, comprising the following steps (1) to (6): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (72) and (73); (2) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of (76) and (71), (76) and (74), or (76) and (75); (3) amplifying gyrB gene DNA from the microorganism using said two pairs of primers to produce two gyrB gene DNA fragments; (4) isolating said two DNA fragments; (5) determining the nucleotide sequences of said two DNA fragments; and (6) identifying the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 7. A method for identifying a microorganism, comprising the following steps (1) to (6): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (77); (2) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of (79) and (71), (79) and (74), or (79) and (75); (3) amplifying gyrB gene DNA from the microorganism using said two pairs of primers to produce two gyrB gene DNA fragments; (4) isolating said two DNA fragments; (5) determining the nucleotide sequences of said two DNA fragments; and (6) identifying the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 8. A method for identifying a microorganism, comprising the following steps (1) to (6): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (77); (2) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of (80) and (71), (80) and (24), or (80) and (75); (3) amplifying gyrB gene DNA from the microorganism using said two pairs of primers to produce two gyrB gene DNA fragments; (4) isolating said two DNA fragments; (5) determining the nucleotide sequences of said two DNA fragments; and (6) identifying the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 9. A method for detecting a microorganism, comprising the following steps (1) to (5): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of the sequence pairs (69) and (74), (69) and (78), (72) and (71), (72) and (74), and (72) and (78); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) isolating said DNA fragment; (4) determining the nucleotide sequence of said DNA fragment; and (5) detecting the microorganism by comparing the nucleotide sequence of said amplified gyrB gene DNA fragment to known gyrB gene DNA fragment sequences.
 10. The method for detecting a microorganism according to claim 9, wherein the amino acid sequence pairs that are used are sequence pairs (69) and (74), (69) and (78), (72) and (74), or (72) and (78); and said microorganism belongs to proteobacteria.
 11. A method for detecting a microorganism, comprising the following steps (1) to (8): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (71); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (73); (4) synthesizing forward and reverse primers based on a single pair of amino acid sequences (70) and (71); (5) amplifying the gyrB gene DNA fragment produced in step (2) using said two primers to produce two gyrB gene DNA fragment; (6) isolating said two DNA fragments; (7) determining the nucleotide sequences of said two DNA fragments; and (8) detecting the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 12. A method for detecting a microorganism, comprising the following steps (1) to (8): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (74); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (73); (4) synthesizing forward and reverse primers based on a single pair of amino acid sequences (70) and (74); (5) amplifying the gyrB gene DNA fragment produced in step (2) using said two pairs of primers, so that two gyrB gene DNA fragments are produced; (6) isolating said two DNA fragments; (7) determining the nucleotide sequences of said two DNA fragments; and (8) detecting the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 13. A method for detecting a microorganism comprising the following steps (1) to (8): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (72) and (74); (2) amplifying gyrB gene DNA from the microorganism using said two primers to produce a gyrB gene DNA fragment; (3) synthesizing forward and reverse primers based on a single pair of amino acid sequences (72) and (73); (4) synthesizing forward and reverse primers based on a single pair of amino acid sequences (70) and (74); (5) amplifying the gyrB gene DNA fragment produced in step (2) using said two pairs of primers, so that two gyrB gene DNA fragments are produced; (6) isolating said two DNA fragments; (7) determining the nucleotide sequences of said two DNA fragments; and (8) detecting the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 14. A method for detecting a microorganism, comprising the following steps (1) to (6): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (72) and (73); (2) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of (76) and (71), (76) and (74), or (76) and (75); (3) amplifying gyrB gene DNA from the microorganism using said two pairs of primers to produce two gyrB gene DNA fragments; (4) isolating said two DNA fragments; (5) determining the nucleotide sequences of said two DNA fragments; and (6) detecting the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 15. A method for detecting a microorganism, comprising the following steps (1) to (6): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (77); (2) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of (79) and (71), (79) and (74), or (79) and (75); (3) amplifying gyrB gene DNA from the microorganism using said two pairs of primers to produce two gyrB gene DNA fragments; (4) isolating said two DNA fragments; (5) determining the nucleotide sequences of said two DNA fragments; and (6) detecting the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences.
 16. A method for detecting a microorganism, comprising the following steps (1) to (6): (1) synthesizing forward and reverse primers based on a single pair of amino acid sequences (69) and (77); (2) synthesizing forward and reverse primers based on a single pair of amino acid sequences selected from the group consisting of (80) and (71), (80) and (74), or (80) and (75); (3) amplifying gyrB gene DNA from the microorganism using said two pairs of primers to produce two gyrB gene DNA fragments; (4) isolating said two DNA fragments; (5) determining the nucleotide sequences of said two DNA fragments; and (6) detecting the microorganism by comparing the sequences of said two gyrB gene DNA fragments to known gyrB gene DNA fragment sequences. 